EP1221965A1 - Use of tgf beta and growth factors in the treatment and prevention of diseases of the intestinal mucosa - Google Patents
Use of tgf beta and growth factors in the treatment and prevention of diseases of the intestinal mucosaInfo
- Publication number
- EP1221965A1 EP1221965A1 EP00971890A EP00971890A EP1221965A1 EP 1221965 A1 EP1221965 A1 EP 1221965A1 EP 00971890 A EP00971890 A EP 00971890A EP 00971890 A EP00971890 A EP 00971890A EP 1221965 A1 EP1221965 A1 EP 1221965A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- pharmaceutical composition
- tgf
- fibres
- use according
- igf
- Prior art date
- Legal status (The legal status 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 status listed.)
- Ceased
Links
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/18—Growth factors; Growth regulators
- A61K38/1841—Transforming growth factor [TGF]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/88—Liliopsida (monocotyledons)
- A61K36/899—Poaceae or Gramineae (Grass family), e.g. bamboo, corn or sugar cane
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/22—Hormones
- A61K38/30—Insulin-like growth factors, i.e. somatomedins, e.g. IGF-1, IGF-2
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- A61K38/40—Transferrins, e.g. lactoferrins, ovotransferrins
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/12—Antidiarrhoeals
Definitions
- the present invention relates to the use of a composition containing transforming growth factor ⁇ (TGF- ⁇ ) and a composition containing anabolic growth factors (AGF), in particular insulin-like growth factor 1 (IGF-1) for the prevention or treatment of malfunction or disease of the intestinal mucosa.
- TGF- ⁇ transforming growth factor ⁇
- AMF anabolic growth factors
- IGF-1 insulin-like growth factor 1
- the invention further relates to a composition containing TGF- ⁇ and specific fibres and/or immunoglobulines and/or calcium which can also be used for such a treatment, in particular in combination with IGF-1.
- the composition containing TGF- ⁇ is administered during a period in which it is desired to inhibit cell proliferation and stimulate cell differentiation.
- the composition containing IGF-1 is administered to restore intestinal epithelial cells.
- TGF- ⁇ is a multifunctional protein found in all mammalian tissues. Currently, five forms of TGF- ⁇ are known, ⁇ l to ⁇ 5. It has been implicated in the development, differentiation and growth of tissue and the control of immune system function and carcinogenesis. TGF- ⁇ can be isolated from natural sources (e.g. blood platelets), mammalian milk or colostrum or can be produced by recombinant cells.
- natural sources e.g. blood platelets
- mammalian milk or colostrum can be produced by recombinant cells.
- IGF-1 is a small protein (molecular weight about 7800) which plays an important role in bone metabolism. It has been shown to stimulate growth of cells in culture. Animal growth is also stimulated in pituitary deficient, normal and catabolic states. Kidney function is also improved. It can be produced using recombinant DNA technology, solid phase peptide synthesis, by isolating it from blood serum or from human or bovine milk.
- TGF- ⁇ and its uses are for instance described in EP 852913.
- This document relates to an enteral food preparation which contains casein rich in TGF- ⁇ 2, a lipid source such as medium chain or long chain triglycerides or polyunsaturated fatty acids and a carbohydrate source, i.e. maltodextrin, corn starch or sucrose.
- This composition is used in the treatment or prophylaxis of inflammatory conditions of the gastrointestinal tract, such as Crohn's disease.
- EP 462,398 describes the combination of TGF- ⁇ 1 and a polyunsaturated fatty acid (PUFA) such as linoleic acid, alpha-linolenic acid, gamma-linolenic acid, arachidonic acid, dihomo- gamma-linolenic acid, eicosapentaenoic acid and/or docosahexanoic acid and/or a derivative thereof for treatment of neoplastic diseases.
- PUFA polyunsaturated fatty acid
- WO 96/34614 describes a method for preventing and/or treating damage to the lining of the alimentary tract resulting from chemotherapy and/or radiation, wherein a milk product extract including a mixture of cell growth factors is administered to a patient.
- the milk product extract preferably a cheese whey extract, may contain lactoferrin and lactoperoxidase and it can be supplemented with growth factors such as IGF-1, IGF-2, TGF- ⁇ , TGF- ⁇ , EGF, PDGF, FGF or KGF. This document does not mention which of the substances mentioned should be present in order to achieve the desired preventing or curing effect.
- TGF- ⁇ 3 Treatment of chemotherapy induced ulcerative mucositis by transforming growth factor ⁇ 3
- Topical application of TGF- ⁇ 3 to the oral mucosa of the Syrian golden hamster prior to chemotherapy significantly reduced the incidence, severity and duration of oral mucositis, reduced chemotherapy associated weight loss and increased survival.
- Prevention of mucositis according to this document is based on limiting the rate of basal epithelial cell proliferation by prior administration of a negative growth regulator.
- TGF- ⁇ 3 can be administered to slow growth of normal cells and thereby inhibit cytotoxic poisoning of the normal cells in the subject.
- the TGF- ⁇ 3 is administered prior to anti-neoplastic therapy.
- a mitogen for epithelial cells can be administered.
- the drawback of the method of this document is that preferably a growth factor obtained by recombinant technology is used.
- these type of growth factors have shown to be less stable during sterilisation treatments. Also the biological availability of these growth factors in the gastrointestinal tract is not yet satisfactory.
- TGF- ⁇ should be administered without the presence of IGF-1, in particular any anabolic growth factor, during the chemotherapy or radiotherapy.
- IGF-1 in particular any anabolic growth factor
- damaging effects that may have occurred during this therapy can be treated by administering anabolic growth factors, in particular IGF-1 in the substantial absence of TGF- ⁇ .
- IBD inflammatory bowel diseases
- the present invention therefore provides the use of TGF- ⁇ and AGF in the preparation of a product for use in the treatment and/or prevention of malfunction or disease of the intestinal mucosa; the product comprising: a) a first pharmaceutical composition comprising TGF- ⁇ in the substantial absence of IGF-1, which TGF- ⁇ is obtained by extraction from a mammalian milk product; b) a second pharmaceutical composition comprising AGF in the substantial absence of TGF- ⁇ , wherein the first and second composition are administered sequentially.
- the weight ratio TGF- ⁇ /IGF-1 in the first pharmaceutical composition is at least 100.
- TGF- ⁇ when a mixture of growth factors is used, for instance when a milk product extract is used, the beneficial effect of TGF- ⁇ is reduced by the presence of anabolic growth factors Therefore, it is preferred to administer TGF- ⁇ in the substantial absence of such growth factors.
- the first pharmaceutical composition comprises TGF- ⁇ in substantial absence of AGF.
- IGF-1 insulin-like growth factor 2
- IGF-2 insulin-like growth factor 2
- EGF epidermal growth factor
- TGF- ⁇ transforming growth factor ⁇
- MMGF mammalian milk growth factor
- FGF fibroblast growth factor
- EGF is for instance described in EP 0546 068, MMGF in WO 99/24470.
- the ratio TGF- ⁇ /AGF is preferably at least 50.
- the AGF in the second pharmaceutical composition is IGF-1. This means that preferably at least IGF- 1 is present in the second composition.
- these include also the active peptide analogues of these growth factors.
- peptide analogue is meant any peptide having substantially the same activity as the growth factor, particularly any peptide analogue which is 90% or more homologous with the growth factor.
- “Pharmaceutical composition” is meant to include any conventional pharmaceutical preparation such as a capsule, a tablet etc., as well as dietetic preparations such as feed supplements or total feeds.
- the sequential administration of the first pharmaceutical composition containing TGF- ⁇ and the second pharmaceutical composition containing AGF, preferably at least IGF-1, according to the invention is particular suitable for intestinal disorders in which two phases can be distinguished.
- the first phase is a phase in which it is desired to inhibit the metabolism.
- the second phase which follows the first phase, the intestinal epithelial cells need to be restored.
- the composition containing TGF- ⁇ is administered during the first phase, the composition containing anabolic growth factors, in particular IGF-1 during the second phase.
- the sequential administration of TGF- ⁇ and IGF-1 is used for the prevention and/or treatment of damage of the intestinal mucosa as a result of chemotherapy and/or radiotherapy.
- damage is meant any alteration in normal structure or function. Such damage includes mucositis, at least partial loss of mucosal crypt area and/or mucosal villus length, or an increase in bacterial translocation across the alimentary tract.
- Chemotherapy and/or radiotherapy are effective at destroying tumours because they target fast-growing tissues. While tumour cells are selectively targeted by anticancer treatments the fast growing tissues of the host are also susceptible, particularly the immune cells of the body and the lining of the alimentary tract. This can result in damage to the linings of the mouth and oesophagus (mucositis, also referred to as stomatitis) and damage to the intestinal lining, commonly in the small bowel and less frequently in the large bowel, leading to severe diarrhoea and pain.
- mucositis also referred to as stomatitis
- a first composition containing TGF- ⁇ should be administered without the presence of IGF-I, preferably any anabolic growth factor, during the chemotherapy or radiotherapy, in particular during at least the period starting at the latest the first day of said chemotherapy or radiotherapy treatment and ending at the latest the last day of treatment. It was furthermore found that after the chemotherapy or radiotherapy, damaging effects that may have occurred during these therapies can be treated by administering a second composition containing AGF, in particular IGF-1, in the substantial absence of TGF- ⁇ .
- IGF-I preferably any anabolic growth factor
- the sequential administration of TGF- ⁇ and IGF-1 is used in the prevention and/or treatment of inflammatory conditions of the intestine, in particular inflammatory bowel diseases (IBD), such as Crohn's disease.
- IBD inflammatory bowel diseases
- TGF- ⁇ a TGF- ⁇ extracted from a mammalian milk product, such as milk or whey, in particular bovine milk or whey, most preferably whey is used.
- a mammalian milk product such as milk or whey, in particular bovine milk or whey, most preferably whey is used.
- the advantages of such TGF- ⁇ are that it comes from a natural source because of the reluctance against products obtained by recombinant techniques, cost effectiveness and the presence of other beneficial components in milk or whey extract, such as immunoglobulins.
- Milk contains TGF- ⁇ l(ca. 15%) and TGF- ⁇ 2 (ca. 85%).
- a process for extracting such a TGF- ⁇ is described in a copending application of the applicants (PCT NL/99/00621).
- an extract which contains binding factors for TGF- ⁇ .
- This extract can be obtained by using an extraction process, preferably excluding acidic extraction steps (pH ⁇ 5.5).
- Binding factors for TGF- ⁇ are defined as components that are able to form a stable complex with TGF- ⁇ in aqueous media. In bovine milk these are albumin and Latency Associated Peptide (LAP).
- binding factors results in increased stability of the growth factor, for instance during sterilisation. It also results in better bioavailability of TGF- ⁇ and thus in higher activity.
- the binding factors help survive the growth factors during passage in the intestine, where digestive enzymes may degrade the growth factors resulting in (partial) loss of activity.
- milk products could be used as a source for growth factors in the treatment of the disorders as mentioned in the present application, but that in order to be useful a separation treatment should be carried out, separating the transforming growth factor from anabolic growth factors.
- a TGF- ⁇ obtained from bovine whey or milk will in general contain more than 100, preferably more than 700 ⁇ g TGF- ⁇ per g protein. Such an extract will for instance contain 750 ⁇ g TGF- ⁇ /g protein.
- the IGF-1 content in this extract will be less than 4, preferably less than 1 ⁇ g/g protein.
- the TGF- ⁇ is present in the composition in such an amount that 50 ng to 150 ⁇ g per day is administered. In case of a liquid product, this will contain TGF- ⁇ in a concentration of 0.5 ⁇ g -1.5 mg TGF- ⁇ per litre. The patient will be administered about 100 ml per day of such a liquid product.
- the first pharmaceutical composition according to the invention also con- tains fibres which upon fermentation form more than 15 g of butyrate per 100 g of short chain fatty acids, preferably more than 20 g of butyrate per 100 g of short chain fatty acids.
- This characteristic means that the composition should contain fibres that release a relative large amount of butyrate when they are fermented in the intestine (colon). The amount of butyrate can be determined by the method described in Journal of Clinical Nutrition, 1991, no. 53, p. 1418-1424.
- fibres which upon fermentation result in butyrate.
- Such fibres are: resistant starch, oats bran, in particular the arabinoxylan rich fraction that is poor in ⁇ -glucan, some soy fibre extracts and wheat bran.
- wheat bran is used.
- the amount of fibre is such that a daily ratio of 1 to 30 g, preferably 3 to 10 g, is obtained. In a liquid preparation the concentration is thus 10 to 300 g/1.
- the TGF- ⁇ composition according to the invention preferably contains immunoglobulins, more in particular in combination with the above mentioned fibres. Their main function is to interact with harmful micro-organisms such as bacteria. This prevents the micro-organism from entering the blood circulation system. This situation in particular occurs when the intestinal mucosa of the patient has been damaged as a result of treatment with chemotherapy.
- the immunoglobulins can be isolated from milk of mammals which have been hyperimmu- nised against certain pathogens or they can be isolated from normal bovine whey or milk. With the process described in the above mentioned patent application, using normal cow's milk as a starting material, a preparation is obtained rich in IgG and IgA. 30 to 50 % of the protein fraction consists of immunoglobulins of the type IgG and IgA. The concentration immunoglobulins in the preparation will, in case of a liquid preparation of 100 ml, be 0.1 to 1500 mg/1.
- the TGF- ⁇ composition contains calcium, preferably in combination with the above mentioned fibres, more preferably in combination with said fibres and immunoglobulins.
- the calcium can be in the form of finely dispersed calcium phosphate, calcium carbonate, calcium citrate or a calcium concentrate from bovine milk.
- the addition of calcium reduces the risk of infection. Calcium lowers the proliferation rate of the epithelial cells.
- the amount of calcium is more than 50 mg/100 ml, preferably more than 100 mg/100 ml, for instances 120 mg/100 ml, based on a liquid composition.
- the first pharmaceutical composition containing TGF- ⁇ according to the invention also contains one or more of the following ingredients: proteins, fat, minerals, trace elements, vitamins, fatty acids and lactoferrin.
- proteins are present in an amount of 3 to 10 % protein equivalents, this includes intact protein, peptides and amino acids.
- the amount of fat is preferably 2 to 10 %, based on the total weight of the preparation.
- the amount of minerals, trace elements and vitamins is according to the daily recommended dosage.
- Vitamin A is vitamin A, C and E.
- Vitamin A and provitamin A are required. Their concentration is preferably more than 130 ⁇ gRE/100 ml, in particular more than 300 ⁇ g/100 ml.
- part of the vitamin A is administered as retinoic acid or a metabolic equivalent thereof.
- Vitamin C and tocopherols are administered because of their role in the antioxidant cascade. During radiotherapy but also with initial inflammatory reactions they can protect the epithelial cells.
- the concentration vitamin C or an equivalent thereof is more than 40 mg/100 ml, preferably more than 60 mg/100 ml.
- the concentration of tocopherols is more than 5 mg, preferably more than 15 mg/100 ml.
- the fats should provide sufficient fatty acids.
- stearidonic acid STA
- Suitable fatty acids and the amounts and ratios in which they are used are described in PCT/EP98/08409, i.e. the fatty acids gamma-linolenic acid, stearidonic acid and eicosapentaenoic acid together constitute 10 to 500 mg/g of the total amount of fatty acids and gamma-linolenic acid and eicosapentaenoic constitute 20 to 50 wt.% and stearidonic acid forms 15 to 50 wt.% of these three fatty acids.
- Lactoferrin can be present because it has anti-bacterial activity against a number of pathogens. This substance can also have a modulating action with initial inflammatory reactions, which are delayed. It is desired to have a daily doses of 0.1 to 3 g of lactoferrin. It is preferred that the composition contains less than 11 %, preferably less than 6 % digestible carbohydrates. A higher percentage of these substances would affect the taste of the composition. Generally about 4.5 g/100 ml are used. As a source of digestible carbohydrates sucrose, but also slowly digestible carbohydrates can be used.
- the dosage of IGF-1 is preferably 0.1 to 100 ⁇ g IGF-1 per kg body weight per day. In a liquid product this concentration is 7 ⁇ g to 7 mg IGF-1 per 100 ml.
- the second composition preferably contains substantially no TGF- ⁇ .
- the ratio IGF-1/TGF- ⁇ is at least 50, preferably at least 100.
- the IGF-1 according to the invention is preferably obtained by extraction from a mammalian milk product, such as milk or whey, in particular bovine milk or whey, most preferably whey. Such an extraction is shown in the copending application of the applicants (PCT/NL/99/00621).
- the second composition can further contain immunoglobulins.
- immunoglobulins In view of the severity of the mucositis which has developed, it is important to prevent and/or treat translocation of harmful substances, for instance micro-organisms. Preferably doses of 0.03 mg to 5 mg immunoglobulins per day are administered. If the IGF-1 is obtained from bovine milk, generally a preparation will be obtained containing 10 to 1000 mg Ig per 100 ⁇ g IGF-1.
- fibres can be present.
- a mixture of fibres is preferably administered.
- theses fibres are soluble non-starch polysaccharides, such as gum arabic or pectin, insoluble non-starch polysaccharides, such as cellulose and hemicel- lulose and oligosaccharides and/or resistant starch and/or lignin.
- soluble non-starch polysaccharides such as gum arabic or pectin
- insoluble non-starch polysaccharides such as cellulose and hemicel- lulose and oligosaccharides and/or resistant starch and/or lignin.
- the second composition can further contain one or more of lactoferrin, glutamine and anti- oxidants.
- Glutamine must have a stable form.
- glutamine rich peptides should be used or extracts from hydrolysates of glutamine rich proteins.
- the amounts of lactoferrin and antioxidants are the same as in the first composition.
- the second composition may contain fat, protein and other microcomponents, such as minerals, vitamins and trace elements. Further, substances that support the total methionin metabolism can be present.
- TGF- ⁇ in the substantial absence of insulin-like growth factor 1 IGF-1, in particular in the absence of AGF, and fibres which upon fermentation form more than 15 g of butyrate per lOOg of short chain fatty acids and/or immunoglobulins are used for preparing a pharmaceutical composition for treatment and/or prevention of malfunction or disease of the intestinal mucosa, more in particular for treatment and/or prevention of damage of the intestinal mucosa as a result of chemotherapy or radiotherapy or for treatment and/or prevention of inflammatory bowel diseases.
- the present invention also relates to a pharmaceutical composition containing TGF- ⁇ in the substantial absence of IGF-1, in particular in the absence of AGF, preferably in combination with fibres which upon fermentation form more than 15 g of butyrate per 100 g of short chain fatty acids and/or immunoglobulins.
- such a composition contains per 100 ml a) 50 ng to 150 ⁇ g TGF- ⁇ b) 1 to 30 g fibres c) 0.01 to 150 mg immunoglobulins d) 0.03 to 1 g lactoferrin e) > 50 mg calcium f) fatty acids g) > 130 ⁇ g RE vitamin A h) > 40 mg vitamin C i) > 5 mg tocopherols j) 3 to 10% protein equivalents
- a suitable liquid TGF- ⁇ based formula contains per 100 ml: a) 4 ⁇ g TGF- ⁇ b) 5 g wheat bran c) 2 mg immunoglobulins d) 0.5 g lactoferrin e) 80 mg calcium f) 4 g fat blend containing 30 % MCT, 26 % palm oil, 16 % soy oil, 8 % borage oil, 11.% echium oil, 6.5 % fish oil and 2.5 % egg lipids g) 300 ⁇ g vitamin A h) 70 mg vitamin C i) 15 mg ⁇ -tocopherol j) 4 g casein k) 5 g maltodextrin Of this formula, 250 ml per day is administered.
- the invention also relates to a pharmaceutical composition containing AGF, preferably IGF- 1, in the substantial absence of TGF- ⁇ and fibres selected from soluble non-starch polysaccharides, such as gum arabic or pectin, insoluble non-starch polysaccharides, such as cellulose and hemicellulose and oligosaccharides and/or resistant starch and/or lignin.
- AGF preferably IGF- 1
- soluble non-starch polysaccharides such as gum arabic or pectin
- insoluble non-starch polysaccharides such as cellulose and hemicellulose and oligosaccharides and/or resistant starch and/or lignin.
- the composition preferably further contains at least one member of the group comprising lactoferrin, glutamine and antioxidants.
- such a composition contains per 100 ml: a) 7 ⁇ g to 7 mg IGF-l b) 1 to 30 g fibres c) 5 to 300 mg immunoglobulins d) 0.3 to 3 g lactoferrin e) 0.5 to 10 g glutamine f) > 130 ⁇ g RE vitamin A g) > 40 mg vitamin C h) > 5 mg tocopherols
- a suitable liquid IGF-1 based formula contains per 100 ml: a) 100 ⁇ g IGF-1 b) 5 g fibre mix: lg wheat bran, 3 g inulin, 1 g oats bran c) 200 mg immunoglobulins d) 0.5 g bovine lactoferrin e) 5 g alanylglutamine f) 300 ⁇ g vitamin A g) 70 mg vitamin C h) 15 mg ⁇ -tocopherol Of this formula, 250 ml per day is administered.
- compositions according to the invention can have the form of any oral preparation, for instance capsules, sachets or tablets each containing a predetermined amount of the active ingredient; powders or granules; solutions or suspensions in an aqueous or non-aqueous liquid.
- Preferred dosage forms are food supplements or total feeds or powders which upon reconstitution with a liquid such as water give a total feed or food supplement.
- the present invention also relates to tube feeds containing these ingredients.
- the present invention also relates to products consisting of a combination of the first compo- sition and the second composition for sequential administration for preventing and/or treating damage of the intestinal mucosa as a result of chemotherapy or radiotherapy or for preventing and/or treating inflammatory conditions of the intestine, in particular Crohn's disease.
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Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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EP07100978A EP1779863A1 (en) | 1999-10-06 | 2000-10-06 | Use of TGF-Beta and growth factors in the treatment and prevention of diseases of the intestinal mucosa |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/NL1999/000620 WO2001024812A1 (en) | 1999-10-06 | 1999-10-06 | USE OF TRANSFORMING GROWTH FACTOR β AND GROWTH FACTORS IN THE TREATMENT AND PREVENTION OF DISEASES OF THE INTESTINAL MUCOSA |
WOPCT/NL99/00620 | 1999-10-06 | ||
PCT/NL2000/000719 WO2001024813A1 (en) | 1999-10-06 | 2000-10-06 | Use of tgf beta and growth factors in the treatment and prevention of diseases of the intestinal mucosa |
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EP07100978A Division EP1779863A1 (en) | 1999-10-06 | 2000-10-06 | Use of TGF-Beta and growth factors in the treatment and prevention of diseases of the intestinal mucosa |
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EP07100978A Withdrawn EP1779863A1 (en) | 1999-10-06 | 2000-10-06 | Use of TGF-Beta and growth factors in the treatment and prevention of diseases of the intestinal mucosa |
EP00971890A Ceased EP1221965A1 (en) | 1999-10-06 | 2000-10-06 | Use of tgf beta and growth factors in the treatment and prevention of diseases of the intestinal mucosa |
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CN117279953A (zh) | 2021-02-16 | 2023-12-22 | 詹森药业有限公司 | 靶向bcma、gprc5d和cd3的三特异性抗体 |
TW202304979A (zh) | 2021-04-07 | 2023-02-01 | 瑞士商諾華公司 | 抗TGFβ抗體及其他治療劑用於治療增殖性疾病之用途 |
TW202309522A (zh) | 2021-05-11 | 2023-03-01 | 美商健生生物科技公司 | 用於監測復發性及/或難治性多發性骨髓瘤之治療的方法及組成物 |
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DE3206784C2 (de) * | 1982-02-25 | 1985-05-09 | Pfrimmer & Co Pharmazeutische Werke Erlangen Gmbh, 8520 Erlangen | Glutaminhaltige Zubereitungen für orale oder intravenöse Applikation |
EP0269408A3 (en) * | 1986-11-26 | 1989-08-30 | Genentech, Inc. | Tgf-beta in the treatment of inflammatory disorders |
US5147854A (en) * | 1990-05-22 | 1992-09-15 | Hoffmann-La Roche Inc. | Tgf-b compositions and method |
US5824297A (en) * | 1990-06-25 | 1998-10-20 | Oncogene Science, Inc. | Tissue-derived tumor growth inhibitors, methods of preparation and uses thereof |
AUPN271295A0 (en) * | 1995-05-02 | 1995-05-25 | Gropep Pty Ltd | Method of treatment |
SE9002732D0 (sv) * | 1990-08-24 | 1990-08-24 | Kabivitrum Ab | Product containing growth factor |
US5817625A (en) * | 1992-09-21 | 1998-10-06 | Oncogene Science, Inc. | Methods of prevention of oral mucositis with transforming growth factor beta |
US5451411A (en) * | 1993-10-15 | 1995-09-19 | University Of Washington | Methods and compositions for the oral delivery of therapeutic agents |
EP0756828B2 (en) * | 1995-08-04 | 2010-09-22 | N.V. Nutricia | Nutritional composition containing fibres |
EP0852913A1 (en) * | 1997-01-14 | 1998-07-15 | Societe Des Produits Nestle S.A. | Composition and method for treatment of inflammatory conditions of the gastro-intestinal tract |
NL1005677C2 (nl) * | 1997-03-27 | 1998-09-29 | Campina Melkunie Bv | Werkwijze voor het winnen van groeifactoren, of een samenstelling die één of meer groeifactoren bevat, uit melk of een derivaat daarvan. |
DE19757414A1 (de) * | 1997-12-23 | 1999-07-01 | Nutricia Nv | Fettmischung |
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- 1999-10-06 WO PCT/NL1999/000620 patent/WO2001024812A1/en active Application Filing
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2000
- 2000-10-06 CN CNB2004100749613A patent/CN1299766C/zh not_active Expired - Fee Related
- 2000-10-06 EP EP07100978A patent/EP1779863A1/en not_active Withdrawn
- 2000-10-06 CN CN00814004A patent/CN1378458A/zh active Pending
- 2000-10-06 BR BR0014563-7A patent/BR0014563A/pt not_active IP Right Cessation
- 2000-10-06 JP JP2001527812A patent/JP2003510367A/ja active Pending
- 2000-10-06 AU AU10632/01A patent/AU1063201A/en not_active Abandoned
- 2000-10-06 WO PCT/NL2000/000719 patent/WO2001024813A1/en not_active Application Discontinuation
- 2000-10-06 EP EP00971890A patent/EP1221965A1/en not_active Ceased
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AU6232899A (en) | 2001-05-10 |
WO2001024812A1 (en) | 2001-04-12 |
AU1063201A (en) | 2001-05-10 |
WO2001024813A1 (en) | 2001-04-12 |
JP2003510367A (ja) | 2003-03-18 |
CN1626239A (zh) | 2005-06-15 |
BR0014563A (pt) | 2002-06-11 |
CN1299766C (zh) | 2007-02-14 |
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