WO2016040555A1 - Malaria treatment kit and system - Google Patents

Malaria treatment kit and system Download PDF

Info

Publication number
WO2016040555A1
WO2016040555A1 PCT/US2015/049305 US2015049305W WO2016040555A1 WO 2016040555 A1 WO2016040555 A1 WO 2016040555A1 US 2015049305 W US2015049305 W US 2015049305W WO 2016040555 A1 WO2016040555 A1 WO 2016040555A1
Authority
WO
WIPO (PCT)
Prior art keywords
effective amount
malaria
kit
artemether
act
Prior art date
Application number
PCT/US2015/049305
Other languages
French (fr)
Inventor
Anthony Fedele MUSSO, Jr.
Original Assignee
Malaria Global Initiative, Corp.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Malaria Global Initiative, Corp. filed Critical Malaria Global Initiative, Corp.
Publication of WO2016040555A1 publication Critical patent/WO2016040555A1/en

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4412—Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4433—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with oxygen as a ring hetero atom
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00—Antiparasitic agents
    • A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
    • A61P33/06—Antimalarials
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Definitions

  • the present invention relates to kits and method of using the kits in the treatment of malaria in humans and, more specifically, to systems, methods and kits for rapid effective treatment in the field or healthcare facilities.
  • Malaria is a known mosquito-borne and transmitted infection affecting humans through parasitic Plasmodium.
  • Plasmodium There are at least five known species of Plasmodium known to be transmitted to humans, with P. falciparum and P. vivax being of greater concern because the majority of deaths arise from these two species.
  • P. ovale and P. malariae typically result in milder infections and symptoms.
  • Cerebral malaria, resulting from infections of P. falciparum, is the most severe neurological complication. Patients, who survive cerebral malaria, can have increased risk of deficits in neurological and cognitive abilities, and difficulties with behavior and likelihood of epilepsy in young victims.
  • the life cycle of the malaria-causing Plasmodium begins with an infected female mosquito, i.e. , an Anopheles mosquito (definitive-primary host), which transfers a motile infective sporozoite to a human (secondary host) when the mosquito takes a blood meal from the human.
  • the sporozoite is transferred from the infected mosquito into the human skin through the female mosquito's saliva.
  • the sporozoite then travels through the circulatory system of the human, ultimately reaching the liver cells, where it undergoes asexual reproduction, spawning thousands of merozoites.
  • these infect new red blood cells and begin multiplication cycles which produce 8 to 24 new infective merozoites, resulting in the rupturing of cells and restarting of the infective cycle.
  • a non-infected mosquito can acquire the infection through feeding on infected humans, and thereby having the ability to transmit the infection through a subsequent blood meal taken from the skin of the human.
  • Malaria is prevalent in tropical/subtropical regions around the world, including regions of Sub-Saharan Africa, Asia and the Americas along the equatorial line. Malaria infections in these regions can result in hundreds of thousands to over a million deaths per year. Approximately 3.4 billion people - about half of the population - are at risk of malaria. In 2014, the WHO estimates that 207 million people contracted malaria in 2013. Many of the concerned areas comprise rural areas, with many areas having limited health care facilities and/or limited access to health care and health care facilities. More concerning is the fact that millions of travelers from around the world travel to these regions every year, with tens of thousands to over a million contracting malaria.
  • symptoms similar to an influenza infection can include, for example, joint pain, nausea and vomiting, hemolytic anemia, hemoglobin excretion, convulsion, fever, and headaches.
  • the presentation of symptoms may be similar to that of conditions of intestinal infections, for example. Therefore, diagnosis can be late in the life cycle of the infection at which point the infected patient may not have time for transfer to proper facilities when and where possible. These situations presently occur due to the lack of timely availability of treatments.
  • Embodiments of the present invention solve many of the problems and/or overcome many of the drawbacks and disadvantages of the prior art by providing kits and methods for treating malaria.
  • Embodiments of the present invention may include a malaria treatment kit for use in general settings and advanced, rural and/or isolated areas around the world where malaria infections tend to be and are problematic to travelers and indigenous persons, especially in remote areas that are distant from health care facilities or aid centers.
  • Malaria treatment kits of the present invention may comprise one or more WHO approved malaria treatment drugs and recovery components manufactured and packaged by WHO approved and certified facilities.
  • the malaria treatment kits can comprise, for example, effective doses of malaria treatment drugs including, artemether, artemisinin-based combination therapies (ACT), primaquine, combinations and various forms thereof and various other WHO approved treatment components.
  • the effective doses can be in one or more delivery forms, including, but not limited to, injectable forms, oral forms, sublingual forms, rapid dissolvable forms or combinations and variations thereof. Other forms include tablets, capsules, pills, chewables, liquids, gels, powders, combinations thereof and the like.
  • the malaria treatment kits are provided with effective doses for full course treatments as prescribed for the various malaria infections.
  • the length of course of treatments will depend on the type of malaria infection and is governed by the instructions provided with the malaria treatment kits.
  • the malaria treatment kit comprises a malaria rapid detection test (RDT) kit for determining the type of malaria infection in the individual.
  • RDT malaria rapid detection test
  • the malaria treatment kits comprise a comprehensive set or sets of instructions for use of each of the WHO approved drugs and components, including, but not limited to, procedures for treating an individual exhibiting symptoms of malaria infection and procedures for diagnosing the presence of a malaria infection and type of malaria infection.
  • Other embodiments encompassed by the present invention include, rapid rehydration powders for mixing with various liquids or premixed liquid packets, wherein the rehydration components are WHO approved for such uses. These embodiments also encompass instructions for proper use of the rehydration packets.
  • the malaria treatment kits comprise anti-counterfeiting check verification characteristics. These embodiments allow the malaria treatment kit users to verify that the kits are the WHO-approved malaria treatment kits manufactured by WHO approved facilities.
  • kits provide for customer service characteristics for aiding kit users with any questions and comments pertaining to use of the kits in treating individuals or addressing various governmental, regional, and local rules and regulations pertaining to the kits.
  • the some embodiments include customizable kits for distribution in different areas requiring certain rules and regulations be met prior to distribution of malaria treatment kits of the present invention.
  • inventions for using the malaria treatment kits include instructions and method steps for effectively and timely diagnosing and treating individuals exhibiting symptoms of a malaria infection, wherein the instruction manual or manuals, address preferred drug treatment regimens and treatment of secondary symptoms common to the various types of malaria infections.
  • Certain embodiments include packaging requirements that insure adequate preservation of the various components within the malaria treatment kits as well as the kit overall. Additional features, advantages, and embodiments of the invention are set forth or apparent from consideration of the following detailed description, drawings and claims. Moreover, it is to be understood that both the foregoing summary of the invention and the following detailed description are exemplary and intended to provide further explanation without limiting the scope of the invention as claimed.
  • Kits and methods are described for rapid and effective treatment of malaria.
  • the kits and methods described herein may be used in different areas and settings, including, for example, in areas where malaria infections are prevalent, rural areas, health care facilities, pseudo- and temporary health care facilities, by health care providers, caregivers and individuals, and others.
  • kits and methods are described in the general context of kits comprising components necessary for diagnosis, treatment and follow-up processing of individuals infected with malaria at all levels of the infection.
  • the kits typically include one or more components for treating any one of main types of malaria infections as well as components for diagnosing the type of malaria infection in a rapid and effective manner.
  • Key aspects include, but are not limited to, WHO-approved malaria treatment components from WHO-approved facilities, comprehensive instructions for insuring best treatment approach and use of the kits, anti-counterfeiting and verification characteristics, customer support characteristics, and kit customization for meeting and abiding by different governmental, regional and local rules and requirements without deviating from the WHO requirements for the kit components.
  • kits comprise everything for treatment of the various types of malaria and conditions of the patient from diagnosis to hydration to appropriate medicine - all within minutes. It effectively handles the emergency conditions of patients suffering from cerebral or severe falciparum. In a timely manner, one can be treated or self-treated for emergency condition, thereby saving lives and decreasing mortality numbers. Therefore, global distribution of the kits of present invention to areas around the world with high malarial concerns can save lives. While the kits and methods are described in the foregoing context, further requirements described hereinafter may also be implemented in the kits and/or methods.
  • the malaria treatment (or malaria survival) kits comprise an effective amount of artemether.
  • This drug is WHO-approved and is highly effective against both malarial parasites P. falciparum and P. vivax. WHO guidelines recommend artemisinin- based combination therapy (ACT), where uncomplicated/afc/param malaria is involved.
  • ACT artemisinin- based combination therapy
  • the artemether-form is used in the ACT and provided as such in the kit.
  • the ACT therefore, would include artemether and lumefantrine in a fixed-dose combination.
  • Lumefantrine is an antimalarial agent used to treat acute uncomplicated malaria. It is administered in combination with artemether for improved efficacy.
  • This combination therapy exerts its effects against the erythrocytic stages of Plasmodium spp. and may be used to treat infections caused by P. falciparum and infections acquired in chloroquine-resistant areas.
  • the ACT is also on the WHO's Essential Medicines list.
  • the ACT, artemether and/or lumefantrine can be in many delivery forms for purposes of the present invention, including, but not limited to, tablets, capsules, dispersibles, pills and the like.
  • kits can include artesunate, as another antimalarial agent.
  • the artesunate can be in tablet form (e.g. , 50 mg), or powder form for injection (e.g. , 60 mg) of anhydrous artesunate in 1-ml ampoules + 5% sodium bicarbonate in 0.6-ml ampoule.
  • Artesunate is a water-soluble hemisuccinate derivative of artemisinin. It is unstable in neutral solution and the injectable formulation must be prepared immediately before use in 5% (w/v) sodium bicarbonate solution to produce the salt sodium artesunate. After parenteral administration, it is rapidly hydrolyzed to the active metabolite
  • dihydroartemisinin The oral formulation is probably hydrolyzed completely before entering the systemic circulation. Artesunate has been reported to clear fever in patients with severe falciparum malaria 16-25 hours after parenteral administration. Oral is recommended for treatment of uncomplicated falciparum malaria in areas where there is evidence of chloroquine, pyrimethamine/sulfadoxine, mefloquine and quinine resistance. For example, adults and children over six months it is recommended that treatment begin with 5 mg/kg orally on the first day followed by 2.5 mg/kg on the second and third days in combination with mefloquine (e.g. , 15 mg/kg) in a single dose on the second day. In a few areas, a higher dose (25 mg/kg) of mefloquine may be required for a cure to be obtained. Oral artesunate should not be used during the first trimester of pregnancy.
  • Parenteral treatment is recommended for treatment of severe falciparum in areas where there is evidence of quinine resistance. Radical cure is then effected with a full course of an effective oral antimalarial treatment regimen.
  • the powder for injection should be reconstituted with 5% sodium bicarbonate and diluted in an equal volume of physiological saline or 5% (w/v) glucose. It should be administered immediately by either intravenous or intramuscular injection. A loading dose of 2 mg/kg should followed by 1 mg/kg after 4 hours and 24 hours. Thereafter, a dose of 1 mg/kg should be given daily until the patient is able to tolerate oral artesunate or for a maximum of 7 days.
  • Parenteral artesunate should be used for the treatment of severe falciparum malaria only where there is evidence that the antimalarial efficacy of quinine is declining.
  • the powder for injection is difficult to dissolve and care should be taken to insure that it is completely dissolved before parenteral administration. It should always be used immediately following reconstitution. If the solution is cloudy or a precipitate is present, the parenteral preparation should be discarded. While there is limited information related to use of the parenteral preparations in pregnancy, the parenteral preparations should not be withheld if it is considered life-saving to the mother.
  • kits can comprise primaquine.
  • This drug is to be used in the treatment of P. vivax or P. ovale malaria.
  • Use of the drug in its various forms works to clear dormant liver forms of the parasites once the parasite has been eliminated from the bloodstream. This requires a 14 day course of the drug, which is a radical cure.
  • Treatment of patients with P. vivax or P. ovale infections with the primaquine works to reduce and/or eliminate potential relapses of infection weeks later. Single doses of the drug is used for rapid response against later stage infections oi falciparum. This results in a rapid reduction in transmission, and is useful in combinations with antimalarial drugs focused on earlier stages of infection.
  • Kits of the present invention may include prevent doses and/or treatment doses of primaquine.
  • primaquine present in packets of single doses (0.25 mg/kg) is safe to give for purposes of preventing transmission of falciparum malaria.
  • primaquine is contraindicated due to the unknown glucose-6- phosphate dehydrogenase status of the fetus.
  • primaquine doses are always expressed as a base but not as a salt.
  • kits of the present invention can comprise one or more deliverable forms of artemether.
  • the ACT can be in the form of a tablet, pill or capsule.
  • the kits provide ACT and instructions for its use wherein the ACT is a four day treatment course delivering the necessary amounts of the drugs to effectively treat the malaria.
  • the primaquine can be in a delivery form of a tablet capsule or pill.
  • Primaquine delivery forms can be formulated to deliver an effective amount of the drug for a two week (14 days) treatment course. In all cases, the delivery forms of the drugs are formulated to deliver an effective amount of the drug for the purposes of treating the patient infected with or suspected of malarial infection.
  • the effective doses can be in one or more delivery forms, including, but not limited to, injectable forms, oral forms, sublingual forms, rapid dissolvable forms or combinations and variations thereof.
  • Other forms include tablets, capsules, pills, chewables, liquids, gels, powders, combinations thereof and the like.
  • the kits provide instructions for use of the drugs for effective life saving measures.
  • Table 1 illustrates WHO-approved malarial treatment drugs and combinations, including formulation and strengths, as well as packaging descriptions. These may be used in any necessary combination depending on any number of factors including, but not limited to, local, regional and governmental regulations and approvals, requirements for treatments of particularly prevalent forms of malaria infections and/or various types of resistance to known treatments:
  • Artesunate Powder for injection 30mg Vial 1 vial of artesunate powder is co-packed with 1 ampoule of sodium bicarbonate injection (0.5mL:25mg) and 1 ampoule of sodium chloride injection (2.5mL:22.5mg)
  • kits can comprise additional components necessary in the treatment and/or diagnosis of the malaria infection.
  • the kit comprises a malaria rapid test kit. Instructions are provided for using the malaria test kits.
  • the kits of the present invention can provide a malaria rapid test kit capable of diagnosis within 15-20 minutes of opening the malaria treatment kit.
  • the patient can be effectively diagnosed through a care giver, for example, or self-diagnosed, and started on a treatment course by a self or a care giver, e.g. , clinician or care giver.
  • the ability to rapidly test and begin immediate treatment with the malaria specific drug from the malaria treatment kit greatly enhances survival chances and minimizes unnecessary organ damage from lack of proper and timely treatment.
  • a standard malaria test kit the tester will be instructed to collect whole blood specimens following regular clinical laboratory procedures and store specimens in a refrigerator if not used the same day. A 0.1% of sodium azide can be added to specimens as a preservative without affecting results of the assay. Store as packaged in a sealed pouch at 2-30 degrees C and not in direct sunlight. The test is stable through the expiration date printed on the sealed pouch. The test must remain in the sealed pouch until use and should not be frozen. Collection should be at room
  • Collection can be done by the patient or care provider or other personnel by taking blood sample from the finger using the supplied lancet, test cassette, sealed pouch and sample diluents. Applying sufficient amounts of sample diluents is essential for a valid test result. Adjustments to amounts of diluents may be necessary to insure a proper and timely test result.
  • the instructions will provide for such steps, e.g. , if migration (the wetting of membrane of the cassette) is not observed in the test window after one minute, add one more drop of the kit- supplied diluent to the sample. A positive result could appear as soon as one minute for a sample with high levels of malaria, but results should not be interpreted after 30 minutes.
  • the membranes of the cassettes will be marked accordingly for an interpretation of the results.
  • the cassettes may be marked for one or more types of malaria infections.
  • kits may comprise a rapid rehydration powder that can be mixed with a liquid of choosing or a premixed liquid for oral
  • These powders or mixes are meant to provide rehydration to the patient in need or to prepare the infected patient for duration of the infection while under treatment.
  • These liquids may be adapted for intravenous use where patients are unable take oral consumption of the rapid rehydration mixes, i.e. , where the patient is weak, catatonic or comatose.
  • kits include, but not limited to, thermometers, space blankets, treatment logs, patient tags and treatment schedules.
  • the malaria treatment kits of the present invention are designed for use by healthcare providers, aid givers and the like, but are also designed for self-diagnosis and treatment through use of the instructions provided with each kit. This permits the malaria treatment kits to be distributed to remote areas around the world where a patient may be considerable distance from a healthcare facility or aid center. Again, the present invention is equipped to maximize survival of the infected patient.
  • kits are provided with clear instructions on administration of drugs, testing and diagnosis. Therefore, an individual can self-treat if necessary. This can occur in situations where individuals are in remote areas where access to proper facilities are distant and treatment is necessary immediately.
  • kits and/or one or more components of a kit may include one or more systems and/or methods for product tracking and/or anti-counterfeiting.
  • Embodiments may possess the ability to store and/or access transactional activity.
  • systems and methods may consolidate a portion or all transactional activity around one or more individual products and/or packages within a kit and/or one or more packages for the kit as a whole.
  • the transactional activity may be stored and/or accessed as a single, cohesive analytical view with a system for product tracking and/or anti-counterfeiting.
  • Certain embodiments may include a location system. Certain embodiments may include a data storage system. In certain embodiments, systems may include a geo-location system and temporal data storage system for tracking and/or locating one or more products. The systems may allow tracking and/or locating in real-time, near real-time, on demand, at predetermined intervals, etc. depending on specific requirements of users and/or products. Certain embodiments may also include world-wide web (internet) interfaces and applications programming interfaces (APIs) for easy access to analytics and connections with enterprise CRM (Customer Relationship Management), MES (Manufacturing Execution System), ERP (Enterprise Resource Planning) systems. Systems may operate in conjunction with a wide range of product identifiers, including ID barcodes, QR codes, serial or tracking numbers, active/passive RFID, and NFC tags, or any other information coming directly from the product by sensor feeds that are traceable by the systems.
  • product identifiers including ID barcodes, QR codes, serial or tracking numbers, active/passive RFID, and NFC
  • kits, methods and systems may include enhanced semantic product information and may support anti-counterfeiting tracking and/or analysis. Certain embodiments may include alert triggers.
  • Anti-counterfeiting applications and techniques may cover the malaria treatment kit from the point of departure of the malaria treatment kit, to loading for shipment on pallets, boxes, inner cartons and individual component pouches or containers within the malaria treatment kit.
  • Various anti-counterfeiting systems and methods may be used for individual components of a kit or a kit as a whole.
  • anti- counterfeiting systems and methods may include microtags.
  • Microtags may be made of various materials, such as silica (silicon dioxide - Si0 2 ) or other biologically inert materials.
  • the microtag material may be generally recognized as safe (GRAS) by the U.S. Food and Drug Administration (FDA).
  • Microtags may also be safe for the environment. Microtags may have a high melting point and/or a shelf life that meets or exceeds the product lifetime. Microtags may be encoded with a unique spectral pattern to operate as a microscopic bar code. The unique spectral pattern may be predetermined based on required information to be stored in the microtag.
  • the microtags may be applied directly to products and/or incorporated into substrates and coatings. A field reader may be used to very product information directly from the product, such as a dosage unit or other item, without relying on external packaging.
  • the microtags may be included on, in or otherwise associated with the packaging.
  • relevant product information may be provided to a user.
  • Information from the microtags may include, but is not limited to, product, lot number, item number, authorized country of sale, dosage, manufacturing site, manufacturing date, expiration date, etc.
  • the product information may include whether the product is authentic and/or matches context-specific requirements, such as districution channels, territories, and/or packaging data.
  • Systems may allow conversion of the unique spectral codes into an identification number that can be added to a database or other data storage system. This identification number may then be linked to other fields of information as needed.
  • Mictrotags may be read directly by the field reader or may be forensically recovered and/or reconstructed at a laboratory or other facility.
  • TRUTAGTM TRUTAGTM Technologies, 2045 Lauwiliwili Street, Unit 301, Kapolei, HI 96707
  • kits Packaging of the kits is required in all facets to insure maximum shelf life.
  • the individual components of the kits are preserved in own packaging within the kits. This is necessary where only certain components of the kits are required for a particular malaria event.
  • the kits are also capable of being customized to account for specific regions around the world where certain types of malaria are of more concern, or where local, regional or governmental requirements only permit use of certain kit components.
  • the adaptability of kit components is necessary to insure maximum survival in regions of malarial prevalence.

Landscapes

  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)

Abstract

Kits and systems are described for the treatment of malaria in relevant areas of the world. Kits comprise various malaria treating drugs, malaria testing, and hydration components for treatment of the main malarial infections, wherein the malaria treating drugs are WHO approved and treatment regimens are provided with instructions for use of the kits. Systems are provided for insuring the legitimacy of the kits to avoid counterfeiting.

Description

MALARIA TREATMENT KIT AND SYSTEM
FIELD OF THE INVENTION
The present invention relates to kits and method of using the kits in the treatment of malaria in humans and, more specifically, to systems, methods and kits for rapid effective treatment in the field or healthcare facilities.
BACKGROUND OF THE INVENTION
Malaria is a known mosquito-borne and transmitted infection affecting humans through parasitic Plasmodium. There are at least five known species of Plasmodium known to be transmitted to humans, with P. falciparum and P. vivax being of greater concern because the majority of deaths arise from these two species. P. ovale and P. malariae typically result in milder infections and symptoms. Cerebral malaria, resulting from infections of P. falciparum, is the most severe neurological complication. Patients, who survive cerebral malaria, can have increased risk of deficits in neurological and cognitive abilities, and difficulties with behavior and likelihood of epilepsy in young victims.
As it relates to human infection, the life cycle of the malaria-causing Plasmodium begins with an infected female mosquito, i.e. , an Anopheles mosquito (definitive-primary host), which transfers a motile infective sporozoite to a human (secondary host) when the mosquito takes a blood meal from the human. The sporozoite is transferred from the infected mosquito into the human skin through the female mosquito's saliva. The sporozoite then travels through the circulatory system of the human, ultimately reaching the liver cells, where it undergoes asexual reproduction, spawning thousands of merozoites. In turn, these infect new red blood cells and begin multiplication cycles, which produce 8 to 24 new infective merozoites, resulting in the rupturing of cells and restarting of the infective cycle. Once a human is infected, or other vertebrates targeted by these mosquitoes, a non-infected mosquito can acquire the infection through feeding on infected humans, and thereby having the ability to transmit the infection through a subsequent blood meal taken from the skin of the human.
Malaria is prevalent in tropical/subtropical regions around the world, including regions of Sub-Saharan Africa, Asia and the Americas along the equatorial line. Malaria infections in these regions can result in hundreds of thousands to over a million deaths per year. Approximately 3.4 billion people - about half of the population - are at risk of malaria. In 2014, the WHO estimates that 207 million people contracted malaria in 2013. Many of the concerned areas comprise rural areas, with many areas having limited health care facilities and/or limited access to health care and health care facilities. More concerning is the fact that millions of travelers from around the world travel to these regions every year, with tens of thousands to over a million contracting malaria. Given the known life cycle of the infection, many of these travelers can become infected and return to their home countries before they are diagnosed with malaria. For those persons indigenous to these regions, obtaining proper or correct treatment can be challenging given the limited facilities and/or resources (e.g. , medications, testing equipment, patient care over time of required treatment). Untreated humans become symptomatic within one to three weeks, once infected.
Many exhibit symptoms similar to an influenza infection. Such other symptoms can include, for example, joint pain, nausea and vomiting, hemolytic anemia, hemoglobin excretion, convulsion, fever, and headaches. The presentation of symptoms may be similar to that of conditions of intestinal infections, for example. Therefore, diagnosis can be late in the life cycle of the infection at which point the infected patient may not have time for transfer to proper facilities when and where possible. These situations presently occur due to the lack of timely availability of treatments.
Time is of the essence when the patient is presented later in the infection. For example, infection with P. falciparum can lead to cerebral malaria, which can result in long term detrimental effects and death. The World Health Organization (WHO) classifies malaria as either severe or uncomplicated, from which P. falciparum- aisida. is classified as severe. Because of the third-world conditions in many of these locations, there is a need for a rapid treatment kit that prepares the health care providers, caregivers, leaders and individuals the ability to treat and diagnose malarial infections in a timely and effective manner. SUMMARY OF THE INVENTION
Embodiments of the present invention solve many of the problems and/or overcome many of the drawbacks and disadvantages of the prior art by providing kits and methods for treating malaria.
Embodiments of the present invention may include a malaria treatment kit for use in general settings and advanced, rural and/or isolated areas around the world where malaria infections tend to be and are problematic to travelers and indigenous persons, especially in remote areas that are distant from health care facilities or aid centers. Malaria treatment kits of the present invention may comprise one or more WHO approved malaria treatment drugs and recovery components manufactured and packaged by WHO approved and certified facilities. In certain embodiments, the malaria treatment kits can comprise, for example, effective doses of malaria treatment drugs including, artemether, artemisinin-based combination therapies (ACT), primaquine, combinations and various forms thereof and various other WHO approved treatment components. The effective doses can be in one or more delivery forms, including, but not limited to, injectable forms, oral forms, sublingual forms, rapid dissolvable forms or combinations and variations thereof. Other forms include tablets, capsules, pills, chewables, liquids, gels, powders, combinations thereof and the like.
In certain embodiments, the malaria treatment kits are provided with effective doses for full course treatments as prescribed for the various malaria infections. The length of course of treatments will depend on the type of malaria infection and is governed by the instructions provided with the malaria treatment kits. In another embodiment, the malaria treatment kit comprises a malaria rapid detection test (RDT) kit for determining the type of malaria infection in the individual.
In other embodiments, the malaria treatment kits comprise a comprehensive set or sets of instructions for use of each of the WHO approved drugs and components, including, but not limited to, procedures for treating an individual exhibiting symptoms of malaria infection and procedures for diagnosing the presence of a malaria infection and type of malaria infection. Other embodiments encompassed by the present invention include, rapid rehydration powders for mixing with various liquids or premixed liquid packets, wherein the rehydration components are WHO approved for such uses. These embodiments also encompass instructions for proper use of the rehydration packets. In various other embodiments, the malaria treatment kits comprise anti-counterfeiting check verification characteristics. These embodiments allow the malaria treatment kit users to verify that the kits are the WHO-approved malaria treatment kits manufactured by WHO approved facilities. Other embodiments provide for customer service characteristics for aiding kit users with any questions and comments pertaining to use of the kits in treating individuals or addressing various governmental, regional, and local rules and regulations pertaining to the kits. In this capacity, the some embodiments include customizable kits for distribution in different areas requiring certain rules and regulations be met prior to distribution of malaria treatment kits of the present invention.
Also provided are certain embodiments for using the malaria treatment kits. These embodiments include instructions and method steps for effectively and timely diagnosing and treating individuals exhibiting symptoms of a malaria infection, wherein the instruction manual or manuals, address preferred drug treatment regimens and treatment of secondary symptoms common to the various types of malaria infections. Certain embodiments include packaging requirements that insure adequate preservation of the various components within the malaria treatment kits as well as the kit overall. Additional features, advantages, and embodiments of the invention are set forth or apparent from consideration of the following detailed description, drawings and claims. Moreover, it is to be understood that both the foregoing summary of the invention and the following detailed description are exemplary and intended to provide further explanation without limiting the scope of the invention as claimed. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
Kits and methods are described for rapid and effective treatment of malaria. The kits and methods described herein may be used in different areas and settings, including, for example, in areas where malaria infections are prevalent, rural areas, health care facilities, pseudo- and temporary health care facilities, by health care providers, caregivers and individuals, and others.
Although not required, the kits and methods are described in the general context of kits comprising components necessary for diagnosis, treatment and follow-up processing of individuals infected with malaria at all levels of the infection. The kits typically include one or more components for treating any one of main types of malaria infections as well as components for diagnosing the type of malaria infection in a rapid and effective manner. Key aspects include, but are not limited to, WHO-approved malaria treatment components from WHO-approved facilities, comprehensive instructions for insuring best treatment approach and use of the kits, anti-counterfeiting and verification characteristics, customer support characteristics, and kit customization for meeting and abiding by different governmental, regional and local rules and requirements without deviating from the WHO requirements for the kit components. The kits comprise everything for treatment of the various types of malaria and conditions of the patient from diagnosis to hydration to appropriate medicine - all within minutes. It effectively handles the emergency conditions of patients suffering from cerebral or severe falciparum. In a timely manner, one can be treated or self-treated for emergency condition, thereby saving lives and decreasing mortality numbers. Therefore, global distribution of the kits of present invention to areas around the world with high malarial concerns can save lives. While the kits and methods are described in the foregoing context, further requirements described hereinafter may also be implemented in the kits and/or methods.
In certain embodiments, the malaria treatment (or malaria survival) kits comprise an effective amount of artemether. This drug is WHO-approved and is highly effective against both malarial parasites P. falciparum and P. vivax. WHO guidelines recommend artemisinin- based combination therapy (ACT), where uncomplicated/afc/param malaria is involved. In various embodiments, the artemether-form is used in the ACT and provided as such in the kit. The ACT, therefore, would include artemether and lumefantrine in a fixed-dose combination. Lumefantrine is an antimalarial agent used to treat acute uncomplicated malaria. It is administered in combination with artemether for improved efficacy. This combination therapy exerts its effects against the erythrocytic stages of Plasmodium spp. and may be used to treat infections caused by P. falciparum and infections acquired in chloroquine-resistant areas. The ACT is also on the WHO's Essential Medicines list. The ACT, artemether and/or lumefantrine can be in many delivery forms for purposes of the present invention, including, but not limited to, tablets, capsules, dispersibles, pills and the like.
In other embodiments, the kits can include artesunate, as another antimalarial agent. For example, the artesunate can be in tablet form (e.g. , 50 mg), or powder form for injection (e.g. , 60 mg) of anhydrous artesunate in 1-ml ampoules + 5% sodium bicarbonate in 0.6-ml ampoule. Artesunate is a water-soluble hemisuccinate derivative of artemisinin. It is unstable in neutral solution and the injectable formulation must be prepared immediately before use in 5% (w/v) sodium bicarbonate solution to produce the salt sodium artesunate. After parenteral administration, it is rapidly hydrolyzed to the active metabolite
dihydroartemisinin. The oral formulation is probably hydrolyzed completely before entering the systemic circulation. Artesunate has been reported to clear fever in patients with severe falciparum malaria 16-25 hours after parenteral administration. Oral is recommended for treatment of uncomplicated falciparum malaria in areas where there is evidence of chloroquine, pyrimethamine/sulfadoxine, mefloquine and quinine resistance. For example, adults and children over six months it is recommended that treatment begin with 5 mg/kg orally on the first day followed by 2.5 mg/kg on the second and third days in combination with mefloquine (e.g. , 15 mg/kg) in a single dose on the second day. In a few areas, a higher dose (25 mg/kg) of mefloquine may be required for a cure to be obtained. Oral artesunate should not be used during the first trimester of pregnancy.
Parenteral treatment is recommended for treatment of severe falciparum in areas where there is evidence of quinine resistance. Radical cure is then effected with a full course of an effective oral antimalarial treatment regimen. The powder for injection should be reconstituted with 5% sodium bicarbonate and diluted in an equal volume of physiological saline or 5% (w/v) glucose. It should be administered immediately by either intravenous or intramuscular injection. A loading dose of 2 mg/kg should followed by 1 mg/kg after 4 hours and 24 hours. Thereafter, a dose of 1 mg/kg should be given daily until the patient is able to tolerate oral artesunate or for a maximum of 7 days. Parenteral artesunate should be used for the treatment of severe falciparum malaria only where there is evidence that the antimalarial efficacy of quinine is declining. The powder for injection is difficult to dissolve and care should be taken to insure that it is completely dissolved before parenteral administration. It should always be used immediately following reconstitution. If the solution is cloudy or a precipitate is present, the parenteral preparation should be discarded. While there is limited information related to use of the parenteral preparations in pregnancy, the parenteral preparations should not be withheld if it is considered life-saving to the mother.
Storage of the oral and parenteral forms (tablets, pills, capsules, powders, etc.) should be in tightly closed containers and protected from light to protect the shelf life of the products.
In various embodiments, kits can comprise primaquine. This drug is to be used in the treatment of P. vivax or P. ovale malaria. Use of the drug in its various forms, works to clear dormant liver forms of the parasites once the parasite has been eliminated from the bloodstream. This requires a 14 day course of the drug, which is a radical cure. Treatment of patients with P. vivax or P. ovale infections with the primaquine works to reduce and/or eliminate potential relapses of infection weeks later. Single doses of the drug is used for rapid response against later stage infections oi falciparum. This results in a rapid reduction in transmission, and is useful in combinations with antimalarial drugs focused on earlier stages of infection. Kits of the present invention may include prevent doses and/or treatment doses of primaquine. For example, primaquine present in packets of single doses (0.25 mg/kg) is safe to give for purposes of preventing transmission of falciparum malaria. For pregnant patients, it should be noted that primaquine is contraindicated due to the unknown glucose-6- phosphate dehydrogenase status of the fetus. For dosing purposes, primaquine doses are always expressed as a base but not as a salt.
As discussed herein, artemether can be delivered as an injectable, oral, rapid dissolvable, or combinations thereof. Therefore, the kits of the present invention can comprise one or more deliverable forms of artemether. The ACT can be in the form of a tablet, pill or capsule. The kits provide ACT and instructions for its use wherein the ACT is a four day treatment course delivering the necessary amounts of the drugs to effectively treat the malaria. The primaquine can be in a delivery form of a tablet capsule or pill. Primaquine delivery forms can be formulated to deliver an effective amount of the drug for a two week (14 days) treatment course. In all cases, the delivery forms of the drugs are formulated to deliver an effective amount of the drug for the purposes of treating the patient infected with or suspected of malarial infection. The effective doses can be in one or more delivery forms, including, but not limited to, injectable forms, oral forms, sublingual forms, rapid dissolvable forms or combinations and variations thereof. Other forms include tablets, capsules, pills, chewables, liquids, gels, powders, combinations thereof and the like. In all instances, the kits provide instructions for use of the drugs for effective life saving measures.
Table 1 illustrates WHO-approved malarial treatment drugs and combinations, including formulation and strengths, as well as packaging descriptions. These may be used in any necessary combination depending on any number of factors including, but not limited to, local, regional and governmental regulations and approvals, requirements for treatments of particularly prevalent forms of malaria infections and/or various types of resistance to known treatments:
TABLE 1:
Figure imgf000008_0001
Figure imgf000009_0001
sodium chloride injection (5ml:45mg)]
Artesunate Powder for injection 30mg Vial; 1 vial of artesunate powder is co-packed with 1 ampoule of sodium bicarbonate injection (0.5mL:25mg) and 1 ampoule of sodium chloride injection (2.5mL:22.5mg)
Artesunate Powder for injection Vial; 1 vial of artesunate powder is co-packed
120mg with 1 ampoule of sodium bicarbonate injection (2mL: 100mg) and 1 ampoule of sodium chloride injection (10mL:90mg)
Artesunate + [Sulfadoxine + Tablets + Tablets 50mg + PVC/Alu blister 3 + 1 ; 6 + 2
Pyrimethamine] [500mg + 25mg]
Artesunate + Amodiaquine (as Tablets 25mg + 67.5mg Alu/Alu blister 1 x 3
hydrochloride)
Artesunate + Amodiaquine (as Tablets 50mg + 135mg Alu/Alu blister 1 x 3
hydrochloride)
Artesunate + Amodiaquine (as Tablets lOOmg + 270mg Alu/Alu blister 1 x 3, 1 x 6
hydrochloride)
Artesunate + Mefloquine (as Tablets 25mg + 50mg Alu/Alu strip 1 x 3, 2 x 3
hydrochloride)
Artesunate + Mefloquine (as Tablets lOOmg + 200mg Alu/Alu strip 1 x 3, 2 x 3
hydrochloride)
In various other embodiments of the invention, the kits can comprise additional components necessary in the treatment and/or diagnosis of the malaria infection. In one embodiment, the kit comprises a malaria rapid test kit. Instructions are provided for using the malaria test kits. The kits of the present invention can provide a malaria rapid test kit capable of diagnosis within 15-20 minutes of opening the malaria treatment kit. The patient can be effectively diagnosed through a care giver, for example, or self-diagnosed, and started on a treatment course by a self or a care giver, e.g. , clinician or care giver. The ability to rapidly test and begin immediate treatment with the malaria specific drug from the malaria treatment kit greatly enhances survival chances and minimizes unnecessary organ damage from lack of proper and timely treatment. This is appropriate for severe (emergency) malaria conditions to moderate and even relapse malaria conditions caused by vivax. A standard malaria test kit, the tester will be instructed to collect whole blood specimens following regular clinical laboratory procedures and store specimens in a refrigerator if not used the same day. A 0.1% of sodium azide can be added to specimens as a preservative without affecting results of the assay. Store as packaged in a sealed pouch at 2-30 degrees C and not in direct sunlight. The test is stable through the expiration date printed on the sealed pouch. The test must remain in the sealed pouch until use and should not be frozen. Collection should be at room
temperature with the supplied materials being at room temperature as well. Collection can be done by the patient or care provider or other personnel by taking blood sample from the finger using the supplied lancet, test cassette, sealed pouch and sample diluents. Applying sufficient amounts of sample diluents is essential for a valid test result. Adjustments to amounts of diluents may be necessary to insure a proper and timely test result. The instructions will provide for such steps, e.g. , if migration (the wetting of membrane of the cassette) is not observed in the test window after one minute, add one more drop of the kit- supplied diluent to the sample. A positive result could appear as soon as one minute for a sample with high levels of malaria, but results should not be interpreted after 30 minutes. The membranes of the cassettes will be marked accordingly for an interpretation of the results. The cassettes may be marked for one or more types of malaria infections.
As described herein, once the testing begins, one can also simultaneously self-hydrate and not rely on the intravenous hydration that may or may not be available in the patients location. For example, one does not have to rely on the medicine inventory in a hospital or local pharmacy to resolve their condition if the individual has ready access to a malaria treatment kit of the present invention.
In situations where waiting for the results is potentially life threatening for the infected person, treatment should begin immediately to insure that further internal organ damage does not occur. For example, an ACT treatment could begin immediately while waiting for the test results. In other embodiments of the invention, the kits may comprise a rapid rehydration powder that can be mixed with a liquid of choosing or a premixed liquid for oral
consumption. These powders or mixes are meant to provide rehydration to the patient in need or to prepare the infected patient for duration of the infection while under treatment. These liquids may be adapted for intravenous use where patients are unable take oral consumption of the rapid rehydration mixes, i.e. , where the patient is weak, catatonic or comatose.
Other components for use in the kits include, but not limited to, thermometers, space blankets, treatment logs, patient tags and treatment schedules. The malaria treatment kits of the present invention are designed for use by healthcare providers, aid givers and the like, but are also designed for self-diagnosis and treatment through use of the instructions provided with each kit. This permits the malaria treatment kits to be distributed to remote areas around the world where a patient may be considerable distance from a healthcare facility or aid center. Again, the present invention is equipped to maximize survival of the infected patient.
It will be understood that these kits are provided with clear instructions on administration of drugs, testing and diagnosis. Therefore, an individual can self-treat if necessary. This can occur in situations where individuals are in remote areas where access to proper facilities are distant and treatment is necessary immediately.
In certain embodiments, a kit and/or one or more components of a kit may include one or more systems and/or methods for product tracking and/or anti-counterfeiting.
Embodiments may possess the ability to store and/or access transactional activity. In certain embodiments, systems and methods may consolidate a portion or all transactional activity around one or more individual products and/or packages within a kit and/or one or more packages for the kit as a whole. In certain embodiments, the transactional activity may be stored and/or accessed as a single, cohesive analytical view with a system for product tracking and/or anti-counterfeiting.
Certain embodiments may include a location system. Certain embodiments may include a data storage system. In certain embodiments, systems may include a geo-location system and temporal data storage system for tracking and/or locating one or more products. The systems may allow tracking and/or locating in real-time, near real-time, on demand, at predetermined intervals, etc. depending on specific requirements of users and/or products. Certain embodiments may also include world-wide web (internet) interfaces and applications programming interfaces (APIs) for easy access to analytics and connections with enterprise CRM (Customer Relationship Management), MES (Manufacturing Execution System), ERP (Enterprise Resource Planning) systems. Systems may operate in conjunction with a wide range of product identifiers, including ID barcodes, QR codes, serial or tracking numbers, active/passive RFID, and NFC tags, or any other information coming directly from the product by sensor feeds that are traceable by the systems.
The kits, methods and systems may include enhanced semantic product information and may support anti-counterfeiting tracking and/or analysis. Certain embodiments may include alert triggers. Anti-counterfeiting applications and techniques may cover the malaria treatment kit from the point of departure of the malaria treatment kit, to loading for shipment on pallets, boxes, inner cartons and individual component pouches or containers within the malaria treatment kit. Various anti-counterfeiting systems and methods may be used for individual components of a kit or a kit as a whole. In certain embodiments, anti- counterfeiting systems and methods may include microtags. Microtags may be made of various materials, such as silica (silicon dioxide - Si02) or other biologically inert materials. In certain embodiments, the microtag material may be generally recognized as safe (GRAS) by the U.S. Food and Drug Administration (FDA). Microtags may also be safe for the environment. Microtags may have a high melting point and/or a shelf life that meets or exceeds the product lifetime. Microtags may be encoded with a unique spectral pattern to operate as a microscopic bar code. The unique spectral pattern may be predetermined based on required information to be stored in the microtag. The microtags may be applied directly to products and/or incorporated into substrates and coatings. A field reader may be used to very product information directly from the product, such as a dosage unit or other item, without relying on external packaging. In certain embodiments, the microtags may be included on, in or otherwise associated with the packaging. When a field reader locates a product code and a matched is found in one or more databases, relevant product information may be provided to a user. Information from the microtags may include, but is not limited to, product, lot number, item number, authorized country of sale, dosage, manufacturing site, manufacturing date, expiration date, etc. The product information may include whether the product is authentic and/or matches context-specific requirements, such as districution channels, territories, and/or packaging data. Systems may allow conversion of the unique spectral codes into an identification number that can be added to a database or other data storage system. This identification number may then be linked to other fields of information as needed. Mictrotags may be read directly by the field reader or may be forensically recovered and/or reconstructed at a laboratory or other facility. By way of example, one such technology is that provided under the trademark TRUTAG™ (TRUTAG™ Technologies, 2045 Lauwiliwili Street, Unit 301, Kapolei, HI 96707).
Packaging of the kits is required in all facets to insure maximum shelf life. The individual components of the kits are preserved in own packaging within the kits. This is necessary where only certain components of the kits are required for a particular malaria event. The kits are also capable of being customized to account for specific regions around the world where certain types of malaria are of more concern, or where local, regional or governmental requirements only permit use of certain kit components. The adaptability of kit components is necessary to insure maximum survival in regions of malarial prevalence. Although the foregoing description is directed to the preferred embodiments of the invention, it is noted that other variations and modifications will be apparent to those skilled in the art, and may be made without departing from the spirit or scope of the invention. Moreover, features described in connection with one embodiment of the invention may be used in conjunction with other embodiments, even if not explicitly stated above.

Claims

WHAT IS CLAIMED IS:
1. A malaria treatment kit comprising:
an effective amount of artemether;
an effective amount of an artemisinin-based combination therapy (ACT);
an effective amount of primaquine; and
written instructions on proper administration of each effective amount,
wherein the artemether, ACT and primaquine are World Health Organization (WHO) approved medicinal components.
2. The malaria treatment kit of claim 1 , wherein the effective amount of artemether is in a delivery form of an injectable, oral, rapid dissolvable, or combinations thereof. 3. The malaria treatment kit of claim 1, wherein the effective amount of ACT is in a delivery form of a tablet, pill or capsule.
4. The malaria treatment kit of claim 3, wherein the effective amount of ACT is a four day treatment course.
5. The malaria treatment kit of claim 3, wherein the effective amount of ACT is artesunate and lumefantrine.
6. The malaria treatment kit of claim 1 , wherein the effective amount of primaquine is in a tablet, capsule or pill form.
7. The malaria treatment kit of claim 6, wherein the effective amount of primaquine is a two week treatment course. 8. The malaria treatment kit of claim 7, wherein the effective amount of primaquine is effective for treating Plasmodium vivax.
9. The malaria treatment kit of claim 1, further comprising a malaria rapid test kit
(RTK).
10. The malaria treatment kit of claim 1, wherein the components are individually wrapped. 11. The malaria treatment kit of claim 1, further comprising a rapid rehydration powder for mixing with a liquid or premixed liquid for oral consumption.
12. A malaria treatment kit comprising:
an effective amount of artemether;
an effective amount of an artemisinin-based combination therapy (ACT);
an effective amount of primaquine;
written instructions on proper administration of each effective amount; and a counterfeiting check verification,
wherein the counterfeiting check verification demonstrates that the artemether, ACT and primaquine are World Health Organization (WHO) approved medicinal components.
13. The malaria treatment kit of claim 12, further comprising a malaria RTK, rapid rehydration powder for mixing with a liquid or a premixed liquid. 14. The malaria treatment kit of claim 12, wherein components of the malaria test kit are individually packaged within the kit.
15. The malaria treatment kit of claim 12, wherein the counterfeiting check verification is part of packaging of the malaria treatment kit.
16. The malaria treatment kit of claim 12, wherein the counterfeiting check verification is a microtag applied to one or more of the effective amount of artemether, the effective amount of an artemisinin-based combination therapy (ACT), and the effective amount of primaquine.
17. The malaria treatment kit of claim 16, wherein the microtag is a silica microtag with a predetermined spectral pattern.
A method comprising: providing a kit comprising:
an effective amount of artemether;
an effective amount of an artemisinin-based combination therapy
(ACT);
an effective amount of primaquine;
written instructions on proper administration of each effective amount; and
a counterfeiting check verification,
wherein the counterfeiting check verification demonstrates that the artemether, ACT and primaquine are World Health Organization (WHO) approved medicinal components; and
g the instructions provided in the kit to effectively and systemically treat an individual in need of treatment for a malaria infection.
19. The method of claim 18, further comprising the step of using a rapid detection test using manufacturer's instructions contained in the kit for ascertaining which type of malaria infection is present in the individual to be treated.
20. The method of claim 18, further comprising the step of beginning immediate treatment with an effective amount of an artemether injection based on manufacturer's instructions in the kit if the individual exhibits any symptoms of cerebral malaria, wherein the immediate treatment begins while waiting on results from the rapid detection test.
21. The method of claim 18, comprising the step of beginning treatment with artemether pills, tablets or capsules following the artemether injection based on
manufacturer' s instructions in the kit.
22. The method of claim 18, further comprising the step of administering a rapid rehydration system comprising powder packets, wherein WHO approved rapid rehydration powder packets are mixed with a liquid for administration to the individual in need of rehydration.
23. The method of claim 18, further comprising the step of treating the individual with an effective amount of primaquine based on manufacturer' s instructions in the kit, wherein treatment with primaquine only begins when the rapid detection test results in a positive match for vivax malaria in the individual.
24. The method of claim 18, wherein the counterfeiting check verification is part of packaging of the malaria treatment kit.
25. The method of claim 18, wherein the counterfeiting check verification is a microtag applied to one or more of the effective amount of artemether, the effective amount of an artemisinin-based combination therapy (ACT), and the effective amount of primaquine.
26. The method of claim 25, wherein the microtag is a silica microtag with a predetermined spectral pattern.
27. The method of claim 26, further comprising the step of determining the predetermined spectral pattern of the microtag and accessing information regarding at least a portion of the kit.
A malaria treatment kit comprising:
more of the following components:
a malaria rapid test kit (RTK);
an effective amount of an artemisinin-based combination therapy (ACT) , wherein the artemether is a World Health Organization (WHO) approved medical component;
an effective amount of artemether, wherein the artemether is a WHO approved medical component;
an effective amount of primaquine, wherein the artemether is a WHO
approved medical component;
a rapid rehydration powder for mixing with a liquid or premixed liquid for oral consumption; and
written instructions on proper administration of each of the one or more components of the malaria treatment kit.
29. The malaria treatment kit of claim 28, comprising the malarial rapid test kit (RTK), the effective amount of an artemisinin-based combination therapy (ACT), the effective amount of artemether, the effective amount of primaquine, and the rapid rehydration powder.
30. The malaria treatment kit of claim 28, comprising the malarial rapid test kit (RTK), and the effective amount of an artemisinin-based combination therapy (ACT).
31. The malaria treatment kit of claim 28, comprising the malarial rapid test kit (RTK), the effective amount of an artemisinin-based combination therapy (ACT), the effective amount of artemether, and the rapid rehydration powder.
32. The malaria treatment kit of claim 28, comprising the malarial rapid test kit (RTK), the effective amount of an artemisinin-based combination therapy (ACT), and the rapid rehydration powder. 33. The malaria treatment kit of claim 28, comprising the malarial rapid test kit
(RTK), the effective amount of an artemisinin-based combination therapy (ACT), the effective amount of primaquine, and the rapid rehydration powder.
34. The malaria treatment kit of claim 28, further comprising a counterfeiting check verification, wherein the counterfeiting check verification demonstrates that one or more of the effective amount of artemether, the effective amount of an artemisinin-based combination thereapy (ACT), or the effective amount of primaquine are WHO approved medicinal components. 35. The malaria treatment kit of claim 34, wherein the counterfeiting check verification is a microtag applied to one or more of the effective amount of artemether, the effective amount of an artemisinin-based combination therapy (ACT), or the effective amount of primaquine. 36. The malaria treatment kit of claim 35, wherein the microtag is a silica microtag with a predetermined spectral pattern.
PCT/US2015/049305 2014-09-12 2015-09-10 Malaria treatment kit and system WO2016040555A1 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US201462049596P 2014-09-12 2014-09-12
US62/049,596 2014-09-12
US201562102804P 2015-01-13 2015-01-13
US62/102,804 2015-01-13

Publications (1)

Publication Number Publication Date
WO2016040555A1 true WO2016040555A1 (en) 2016-03-17

Family

ID=55459552

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2015/049305 WO2016040555A1 (en) 2014-09-12 2015-09-10 Malaria treatment kit and system

Country Status (1)

Country Link
WO (1) WO2016040555A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR3113586A1 (en) * 2020-08-29 2022-03-04 Bruno Eto New therapeutic use of Fagaricin as a medicine to treat stenoxene haemoprotozoosis in tropical countries

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002048188A1 (en) * 2000-12-14 2002-06-20 The Council Of The Queensland Institute Of Medical Research Plasmodium aldolase polypeptides and nucleic acids
WO2010099607A1 (en) * 2009-03-02 2010-09-10 Fio Corporation Diagnostic test panel for the diagnostic of malaria and severe bacterial infections
WO2012127287A2 (en) * 2011-03-18 2012-09-27 Febris Bio-Tech Limited Compositions and methods for treating multi-drug resistant malaria
US20130004594A1 (en) * 2011-07-01 2013-01-03 Drip Drop, Inc. Oral rehydration composition
US20140119511A1 (en) * 2011-06-15 2014-05-01 Michael Ward Methods of Identifying Original and Counterfeit Articles using Micro X-Ray Diffraction Mapping
US20140256761A1 (en) * 2009-04-22 2014-09-11 Robert Lewis Steele Enhanced artemisinin-based combination therapy for treating parasitic mediated disease

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002048188A1 (en) * 2000-12-14 2002-06-20 The Council Of The Queensland Institute Of Medical Research Plasmodium aldolase polypeptides and nucleic acids
WO2010099607A1 (en) * 2009-03-02 2010-09-10 Fio Corporation Diagnostic test panel for the diagnostic of malaria and severe bacterial infections
US20140256761A1 (en) * 2009-04-22 2014-09-11 Robert Lewis Steele Enhanced artemisinin-based combination therapy for treating parasitic mediated disease
WO2012127287A2 (en) * 2011-03-18 2012-09-27 Febris Bio-Tech Limited Compositions and methods for treating multi-drug resistant malaria
US20140119511A1 (en) * 2011-06-15 2014-05-01 Michael Ward Methods of Identifying Original and Counterfeit Articles using Micro X-Ray Diffraction Mapping
US20130004594A1 (en) * 2011-07-01 2013-01-03 Drip Drop, Inc. Oral rehydration composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR3113586A1 (en) * 2020-08-29 2022-03-04 Bruno Eto New therapeutic use of Fagaricin as a medicine to treat stenoxene haemoprotozoosis in tropical countries

Similar Documents

Publication Publication Date Title
Meydani et al. Vitamin E and respiratory tract infections in elderly nursing home residents: a randomized controlled trial
Haston Guidance for using tafenoquine for prevention and antirelapse therapy for malaria—United States, 2019
Chico et al. Azithromycin plus chloroquine: combination therapy for protection against malaria and sexually transmitted infections in pregnancy
Stohrer et al. Therapeutic efficacy of artemether‐lumefantrine and artesunate‐mefloquine for treatment of uncomplicated Plasmodium falciparum malaria in Luang Namtha Province, Lao People's Democratic Republic
Tinto et al. Effectiveness of artesunate–amodiaquine vs. artemether–lumefantrine for the treatment of uncomplicated falciparum malaria in Nanoro, Burkina Faso: a non‐inferiority randomised trial
Mayxay et al. A phase III, randomized, non-inferiority trial to assess the efficacy and safety of dihydroartemisinin-piperaquine in comparison with artesunate-mefloquine in patients with uncomplicated Plasmodium falciparum malaria in southern Laos
Agudelo Higuita et al. An update on prevention of malaria in travelers
Mischlinger et al. Single dose treatment of malaria-current status and perspectives
Berman Approval of tafenoquine for malaria chemoprophylaxis
DeVos et al. Malaria prophylaxis
Hitch A review of guidelines/guidance from various countries around the world for the prevention and management of travellers’ diarrhoea: a pharmacist’s perspective
Byakika-Kibwika et al. Intravenous artesunate plus Artemisnin based Combination Therapy (ACT) or intravenous quinine plus ACT for treatment of severe malaria in Ugandan children: a randomized controlled clinical trial
Teshome et al. Comparison of home fortification with two iron formulations among Kenyan children: Rationale and design of a placebo-controlled non-inferiority trial
Akpaloo et al. Does the use of dihydroartemisinin‐piperaquine in treating patients with uncomplicated falciparum malaria reduce the risk for recurrent new falciparum infection more than artemether‐lumefantrine?
Shah et al. Severe Plasmodium falciparum malaria treated with investigational artesunate in the United States
WO2016040555A1 (en) Malaria treatment kit and system
Watkins Pharmacology clear & simple: A guide to drug classifications and dosage calculations
Krudsood et al. Dose ranging studies of new artemisinin-piperaquine fixed combinations compared to standard regimens of artemisisnin combination therapies for acute uncomplicated falciparum malaria
Cohen et al. Cardiac arrest with residual blindness after overdose of Tessalon®(benzonatate) perles
Lefevre et al. Novartis Malaria Initiative: best practice example of pharmaceutical industry's engagement in the fight against malaria
Avila et al. Efficacy of mefloquine and mefloquine–artesunate for the treatment of uncomplicated Plasmodium falciparum malaria in the Amazon region of Bolivia
Rodriguez et al. A case of Plasmodium falciparum malaria treated with artesunate in a 55-year-old woman on return to Florida from a visit to Ghana
Young et al. Medicines management for nurses at a glance
Schwartz et al. Travel medicine
Beauchamp et al. Delayed salicylate toxicity in a 17-year-old girl with initially undetectable salicylate concentration 3.9 hours after ingestion

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 15840689

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 15840689

Country of ref document: EP

Kind code of ref document: A1