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
  • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
  • A61K31/409—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil having four such rings, e.g. porphine derivatives, bilirubin, biliverdine
• • 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
  • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
  • A61K31/7088—Compounds having three or more nucleosides or nucleotides
  • A61K31/7105—Natural ribonucleic acids, i.e. containing only riboses attached to adenine, guanine, cytosine or uracil and having 3'-5' phosphodiester links
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K41/00—Medicinal preparations obtained by treating materials with wave energy or particle radiation ; Therapies using these preparations
  • A61K41/0057—Photodynamic therapy with a photosensitizer, i.e. agent able to produce reactive oxygen species upon exposure to light or radiation, e.g. UV or visible light; photocleavage of nucleic acids with an agent
  • A61K41/0071—PDT with porphyrins having exactly 20 ring atoms, i.e. based on the non-expanded tetrapyrrolic ring system, e.g. bacteriochlorin, chlorin-e6, or phthalocyanines
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/0012—Galenical forms characterised by the site of application
  • A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
  • A61K9/0012—Galenical forms characterised by the site of application
  • A61K9/0048—Eye, e.g. artificial tears
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P27/00—Drugs for disorders of the senses
  • A61P27/02—Ophthalmic agents
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
  • C07K16/18—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans
  • C07K16/22—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies against material from animals or humans against growth factors ; against growth regulators
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K9/00—Medicinal preparations characterised by special physical form
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K16/00—Immunoglobulins [IG], e.g. monoclonal or polyclonal antibodies
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K2319/00—Fusion polypeptide
  • C07K2319/30—Non-immunoglobulin-derived peptide or protein having an immunoglobulin constant or Fc region, or a fragment thereof, attached thereto

Definitions

• Age related macular degeneration is a medical condition that usually affects older adults and results in a loss of vision in the center of the visual field (the macula) because of damage to the retina. It occurs in “dry” and “wet” forms. In the dry form, cellular debris called drusen accumulates between the retina and the choroid, and the retina can become detached. In the wet form (wAMD), which is more severe, blood vessels grow up from the choroid behind the retina which is also named choroidal neovascularization (CNV). As a result of CNV the retina can also become detached.
• CNV choroidal neovascularization
• VEGF vascular endothelial growth factor
• wAMD can be also treated with photodynamic therapy with
• Verteporfin® V ® -PDT
• V ® -PDT Verteporfin®
• the CATT research group compared the baseline characteristics, treatment frequency, visual acuity (VA), and morphologic outcomes of eyes with >50% of the lesion composed of blood (B50 group) versus all other eyes (Other group) enrolled in the Comparison of Age-Related Macular Degeneration Treatments Trials (CATT).
• Treatment for the study eye was assigned randomly to either ranibizumab or bevacizumab and to 3 different dosing regimens over a 2-year period. Reading center graders evaluated baseline and follow-up morphology in color fundus photographs, fluorescein angiography (FA), and optical coherence tomography (OCT).
• wAMD there are two subtypes of wAMD: (I) small active CNV lesion - type of wAMD or (II) predominantly active CNV lesion - type of wAMD.
• the location of the lesion can be subfoveal or juxtafoveal affecting the fovea.
• the type of the lesion can be of all subtypes including predominantly classic, minimally classic, or occult.
• Alternate terms for the "predominantly active CNV lesion - type of wAMD” may include: 1) "pCNV wAMD"
• sCNV wAMD is characterized by an active CNV lesion that occupies less than 50% of the total lesion size
• pCNV wAMD is characterized by an active CNV lesion that occupies at least 50% of the total lesion size.
• the location of the lesion can be subfoveal or juxtafoveal affecting the fovea.
• the type of the lesion can be of all subtypes including predominantly classic, minimally classic or occult.
• the size of the active CNV lesion as well as the total lesion size is determined using Fluorescence Angiography (FA) as described in the MPS protocol [Macular Photocoagulation Study Group, Arch Ophthalmol 1991, 109: 1242-1257].
• treatments for wAMD can be also used for the treatment of patients with "sCNV wAMD".
• Such treatment of patients with "sCNV wAMD” may be as follows:
• anti-VEGF therapy refers to all approved and non-approved treatments aiming to attenuate free VEGF in the eye. This includes particularly aflibercept, ranibizumab, bevacizumab, KH-902, and pegaptanib, but is not limited to these compounds.
• Anti-VEGF treatment may be applied according to the following treatment schedules:
• Fluoresceine Angiography Indocyanine Angiography, Funduscopy, etc. stabilizes, followed by discontinuation of treatment. Re-initiation of treatment upon deterioration of visual acuity and/or retinal morphology.
• V ® -PDT Single or repeated applications of photodynamic therapy with Visudyne ®
• V ® -PDT Single or repeated applications of steroids (all available local or systemic application routes) including slow-release or depot formulations (e.g. Ozurdex, triamcinolone, dexamethasone, Iluvien, etc.)
• a total of 304 Chinese subjects with age-related neovascular or wet age-related macular degeneration were enrolled in a randomized, double-blind clinical study to assess the efficacy of intravitreal (IVT) administrated aflibercept compared with V ® -PDT on the mean change in BCVA (Best corrected visual acuity) from baseline to Week 28.
• BCVA of the study eye was assessed according to the standard procedures developed for the ETDRS (Early Treatment Diabetic Retinopathy Study) adapted for Age Related Eye Disease Study (AREDS). The key inclusion criteria were as follows:
• CNV choroidal neovascularization
• juxtafoveal lesions that affect the fovea, as evidenced by fluorescein angiography (FA), in the study eye.
• FA fluorescein angiography
• the area of the CNV had to occupy at least 50% of the total lesion.
• Total lesion size is greater than 12 disc areas (30.5 mm 2 , including blood, scars and
• Sub-retinal hemorrhages that is >50% of the total lesion area, or if the blood is under the fovea and is 1 or more disc areas in size. (If the blood is under the fovea, then the fovea must be surrounded by 270 degrees by visible CNV.)
• PCV polypoidal choroidal vasculopathy
• the lesion size was determined by a central reading center based on the MPS protocol [Macular Photocoagulation Study Group, Arch Ophthalmol 1991, 109: 1242-1257].
• the active CNV size, the area of CNV (mm 2 ) as well as the total lesion size was measured using the FA.
• the central retinal thickness was determined by optical coherence tomography.
• VTE2Q8 group patients were treated with 2 mg (0.05 mL) aflibercept administered intravitreally at baseline, week 4, 8, 16, 24, 32, 40 and 48.
• V ® -PDT was performed at baseline and potential PDT retreatment according to the guidelines for the use of PDT treatment in wAMD [Verteporfin Roundtable Participants, Retina. 2005; 25(2): 119-34] were performed at week 12 and 24.
• subjects in the PDT—VEGF Trap-Eye group received an IVT injection of 2.0 mg VEGF Trap-Eye, followed by additional 2.0 mg VEGF Trap-Eye injections at Weeks 32, 36, 40, and 48.
• Intravitreal injections of 2 mg aflibercept was superior to V ® -PDT with a mean change from baseline BCVA letter score at week 28 of 14.0 (-29 to 59) VTE2Q8 group versus 3.9 (-36 to 43) PDT group (P ⁇ 0.0001) in the whole study population irrespective of the active CNV lesion size.
• FIG 1/2 Mean change from baseline in ETDRS BCVA letter score by visit in subjects with an active CNV lesion > 50% of total lesion size at baseline.
• the mean change in BCVA score (no. of letters) as measured by ETDRS from baseline at week 1 (V3) week 4 (V4), week 8 (V5), week 12 (V6), week 16 (V7), week 20 (V8), week 24 (V9), week 28 (VIO), Week 32 (Visit 11), Week 36 (Visit 12), Week 40 (Visit 13), Week 44 (visit 14), Week 28 (Visit 15), Week 52 (Visit 16) is shown for the VTE2Q8 group (solid line with diamonds) and the PDT->VTE group (dashed line with squares).
• the mean change in BCVA score from baseline is 12.7 for the VTE2Q8 group and 1.5 for the PDT->VTE group.
• the mean change in BCVA score from baseline is 14.0 for the VTE2Q8 group and 6.4 for the PDT->VTE group.
• Figure 2/2 Mean change from baseline in ETDRS BCVA letter score by visit in subjects with an active CNV lesions ⁇ 50% of total lesion size at baseline.
• the mean change in BCVA score (no. of letters) as measured by ETDRS from baseline at week 1 (V3) week 4 (V4), week 8 (V5), week 12 (V6), week 16 (V7), week 20 (V8), week 24 (V9), week 28 (V10), Week 32 (Visit 11), Week 36 (Visit 12), Week 40 (Visit 13), Week 44 (visit 14), Week 28 (Visit 15), Week 52 (Visit 16) is shown for the VTE2Q8 group (solid line with diamonds) and the PD->VTET group (dashed line with squares).
• the mean change in BCVA score from baseline is 16.7 for the VTE2Q8 group and 8.0 for the PDT->VTE group.
• the mean change in BCVA score from baseline is 18.1 for the VTE2Q8 group and 13.4 for the PDT->VTE group.

Landscapes

• Health & Medical Sciences (AREA)
• Chemical & Material Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Medicinal Chemistry (AREA)
• General Health & Medical Sciences (AREA)
• Public Health (AREA)
• Veterinary Medicine (AREA)
• Pharmacology & Pharmacy (AREA)
• Animal Behavior & Ethology (AREA)
• Epidemiology (AREA)
• Molecular Biology (AREA)
• Biochemistry (AREA)
• Organic Chemistry (AREA)
• Gastroenterology & Hepatology (AREA)
• Immunology (AREA)
• Proteomics, Peptides & Aminoacids (AREA)
• Genetics & Genomics (AREA)
• Ophthalmology & Optometry (AREA)
• Biophysics (AREA)
• Dermatology (AREA)
• General Chemical & Material Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Bioinformatics & Cheminformatics (AREA)
• Engineering & Computer Science (AREA)
• Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Medicinal Preparation (AREA)
• Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
• Nitrogen Condensed Heterocyclic Rings (AREA)

Priority Applications (19)

Applications Claiming Priority (4)

Related Child Applications (2)

Publications (1)

Family

ID=55069121

Family Applications (1)

Country Status (16)

Cited By (3)

Families Citing this family (13)

Citations (5)

Family Cites Families (2)

• 2015
  • 2015-12-10 PT PT158199653T patent/PT3230316T/pt unknown
  • 2015-12-10 EP EP21207057.7A patent/EP3985023A1/en active Pending
  • 2015-12-10 HR HRP20220066TT patent/HRP20220066T1/hr unknown
  • 2015-12-10 WO PCT/US2015/065022 patent/WO2016094673A1/en not_active Ceased
  • 2015-12-10 PL PL15819965T patent/PL3230316T3/pl unknown
  • 2015-12-10 JP JP2017530277A patent/JP7320919B2/ja active Active
  • 2015-12-10 CN CN202210019267.XA patent/CN114306575A/zh active Pending
  • 2015-12-10 CN CN201580066980.8A patent/CN106999511A/zh active Pending
  • 2015-12-10 RS RS20220058A patent/RS62827B1/sr unknown
  • 2015-12-10 EP EP15819965.3A patent/EP3230316B1/en active Active
  • 2015-12-10 ES ES15819965T patent/ES2907148T3/es active Active
  • 2015-12-10 DK DK15819965.3T patent/DK3230316T3/da active
  • 2015-12-10 SI SI201531805T patent/SI3230316T1/sl unknown
  • 2015-12-10 AU AU2015360496A patent/AU2015360496B2/en active Active
  • 2015-12-10 CN CN202110181096.6A patent/CN112826934A/zh active Pending
  • 2015-12-10 CA CA2970315A patent/CA2970315C/en active Active
  • 2015-12-10 HU HUE15819965A patent/HUE057653T2/hu unknown
  • 2015-12-10 US US15/534,030 patent/US20170326106A1/en not_active Abandoned
  • 2015-12-10 LT LTEPPCT/US2015/065022T patent/LT3230316T/lt unknown
• 2019
  • 2019-06-26 US US16/453,242 patent/US20190381008A1/en active Pending
• 2020
  • 2020-10-15 JP JP2020173951A patent/JP2021004262A/ja active Pending
• 2021
  • 2021-10-08 AU AU2021107575A patent/AU2021107575A4/en not_active Expired
  • 2021-10-08 AU AU2021245214A patent/AU2021245214B2/en active Active
• 2022
  • 2022-09-26 JP JP2022152791A patent/JP2022183183A/ja active Pending
• 2024
  • 2024-07-31 AU AU2024205237A patent/AU2024205237A1/en active Pending

Patent Citations (5)

Non-Patent Citations (14)

Also Published As

Similar Documents

Legal Events