WO1986000016A1 - Herpes simplex treatment - Google Patents

Herpes simplex treatment Download PDF

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Publication number
WO1986000016A1
WO1986000016A1 PCT/US1984/000920 US8400920W WO8600016A1 WO 1986000016 A1 WO1986000016 A1 WO 1986000016A1 US 8400920 W US8400920 W US 8400920W WO 8600016 A1 WO8600016 A1 WO 8600016A1
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WO
WIPO (PCT)
Prior art keywords
bis
phenol
diacetate
ester
dosage
Prior art date
Application number
PCT/US1984/000920
Other languages
French (fr)
Inventor
Gerald N. Kern
Original Assignee
Medical Technology Corp. Of America, Inc.
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 Medical Technology Corp. Of America, Inc. filed Critical Medical Technology Corp. Of America, Inc.
Priority to JP59502497A priority Critical patent/JPS61502395A/en
Priority to EP19840902564 priority patent/EP0183694A4/en
Priority to PCT/US1984/000920 priority patent/WO1986000016A1/en
Publication of WO1986000016A1 publication Critical patent/WO1986000016A1/en

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/20Antivirals for DNA viruses
    • A61P31/22Antivirals for DNA viruses for herpes viruses

Definitions

  • Herpes Simplex Herpesvirus Hominis
  • Herpes Simplex occurs in two antigenic tyes. Herpes febrilis and Herpes genitalis, referred as Type 1 and Type 2. Infection is usually manifested by the appearance of vesicular eruptions, oral herpetic lesions, commonly referred to as fever blisters, or cold sores about the lips in the instance of Herpes Simplex Type 1, and vesicular lesions on and about the male or female genitalia in the instance of Herpes Simplex Type 2.
  • Persons with Herpes Simplex infections are likely to have recurrent periods of lesion development spaced by periods of remission. Management of the condition involves easing the itching sensation which accompanies the lesion periods, and speeding remission.
  • (p-hydroxyphenyl) phthalide in amounts up to 100 milligrams, preferably 15 to 30 milligrams initially and repetitively at predetermined intervals. Because 3,3-bis (p-hydroxyphenyl) phthalide is a cathartic, there is an unpleasant side effect to its use which suggests reduced usage concentrations, but the patentee does not suggest any lower dosage will be effective in Herpes Simplex management. Summary of the Invention
  • Still other objects include provision of products comprising phenol, 4,4'- (2-pyridinyl methylene) bis diacetate (ester), carriers and therapeutic agents for coapplication with phenol, 4,4'-(2-pyridinyl methylene) bis diacetate (ester).
  • the method includes administering such dosage orally, administering a dosage of from about 0.1 to about 9.5 milligrams of phenol, 4,4'-(2-pyridinyl methylene) bis diacetate (ester), suspending the phenol, 4,4'-(2-pyridinyl methylene) bis,- diacetate (ester) in a carrier for administration, combining the phenol, 4,4'-(2-pyridinyl methylene) bis,- diacetate (ester) with a second therapeutic agent in an effective dosage for administration therewith, e.g.
  • the invention further contemplates provision of a product comprising a dosage of phenol, 4,4'- (2-pyridinyl methylene) bis,- diacetate (ester) effective upon oral ingestion for management of Herpes Simplex, and less than is effective for catharsis of the person receiving the dosage and combined with an ingestible carrier.
  • the product comprises a dosage between 0.1 and 9.5 milligrams, and may further comprise one or more vitamins in effective dosage, preferably free of an enteric coating.
  • Phenol, 4,4'-(2-pyridinyl methylene) bis diacetate (ester), commonly referred to as Bisacodyl is a diphenyl trimethane suitably prepared from 2-pyridine- carboxaldehyde condensed with phenol in the presence of sulfuric acid or other dehydrant, followed by esterification with acetic anhydride and anhydrous sodium acetate, as described in U.S.P. 2,764,590. It is a white to off-white crystalline powder slightly soluble in water but fairly soluble in common organic solvents. It is known to be used as a contact laxative, acting to increase peristalsis throughout the large intestine.
  • a typical dose as a laxative is oral or rectal not less than 10 milligrams and up to 30 milligrams and is administered in an enteric coating to ensure passage to the larage intestine. It is known to inhibit glucose absorption and intestinal Na-K-ATPase activity.
  • the phenol, 4,4'-(2-pyridinyl methylene) bis,- diacetate (ester) may be combined with other therapeutic agents each for its own purpose e.g. to relieve stress, or to enhance the effectiveness of the phenol, 4,4'-(2-pyridinyl methylene) bis,- diacetate (ester) when administered.
  • agents as vitamins A, D, E, C, Folic acid, B-l, B-2, Niacin, B-6, and B-12, among others can be combined with the phenol, 4,4'-(2-pyridinyl methylene) bis diacetate (ester).
  • agents for combining with phenol, 4,4'- ⁇ 2-pyridinyl methylene) bis diacetate (ester) include amino acids, such as lysine and leucine; proteins such as gelatin and gliadin; or carbohydrates, e.g. starch, lactose and the like.
  • the phenol, 4,4'-(2-pyridinyl methylene) bis,- diacetate (ester) may be suitably dispersed in a carrier, e.g. tablet or capsule carriers and components such as excipients, bulking agents, lubricants, disintegrants, dyes and the like as are known in tablet making technology for the purpose of easing the administration of the phenol, 4,4'-(2-pyridinyl methylene) bis diacetate (ester).
  • carrier further embraces vehicles used or useful in preparing injection form of the phenol, 4,4 ⁇ -(2-pyridinyl methylene) bis,- diacetate (ester) products of the invention, such as sesame oil and the like.
  • OMPI capsule 3.35 milligrams of phenol, 4,4'-(2-pyridinyl methylene) bis,- diacetate (ester) with 490 milligrams of an aliquot of a mixture of vitamins comprising:
  • Vitamin A 2500 units Vitamin D 400 units Vitamin E 15 units Vitamin C 60 mg. Folic acid 0.3 mg. Vitamin B-l 1.0 mg. Vitamin B-2 1.2 mg. Niacin 13.5 mg. Vitamin B-6 1.0 mg. Vitamin B-12 4.5 mg. blended with 2 parts of cornstarch per part of vitamin mix.
  • the effective dosage rate for the CONTROL I and II treatments was 30 milligrams per 8 hours for the first day, and a like amount at 12 hour intervals
  • the EXAMPLE I dosage rate was one capsule (3.35 mg. per dosage) every six to eight hours on the first day and thereafter at 8 to 12 hour intervals.
  • vitamins in the EXAMPLE I formulation adds stress relief factors to the formulation to ameliorate the stress which often accompanies onset of a Herpes condition.
  • a second capsule formula of the invention composition was prepared from: phenol, 4,4*-(2-pyridinyl methylene) bis diacetate (ester) 3 . 5 mg . phenacetin 350. mg . chloropheniramine maleate 3. mg . caffein 38. mg . phenylpropanolamine HCL 9. mg . by blending the ingredients eutectically.
  • a tablet form of the invention dosage is prepared by blending phenol, 4,4 • -(2-pyridinyl methylene) bis diacetate (ester), 3.5 mg. , 100 mg. lactose, 100 mg. starch, and 10 mg. talc as a lubricant. It will be noted that this formulation can be packaged in capsule form with the omission of the talc and adjusting the lactose and starch concentration accordingly.
  • a protein containing capsule is prepared by blending eutectically phenol, 4,4'-(2- ⁇ yridinyl methylene) bis diacetate (ester), 3.5 mg. , 200 mg. lactose, 100 mg. gliadin or gelatin protein, and about 100 mg. of the amino acid lysine.
  • An intramuscular injectable formulation is prepared by blending, per dosage, 5 cc. sesame oil, 250 units of Vitamin E, and 5 mg. of phenol, 4,4'-(2-pyridinyl methylene) bis diacetate (ester).

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

Abstract

Method of the effective management of Herpes Simplex including the administration of an effective dosage of phenol, 4,4'-(2-pyridinyl methylene) bis diacetate (ester), in combination with a carrier, vitamins or other therapeutic agents, and an effective dosage product comprising phenol, 4,4'-(2-pyridinyl methylene) bis diacetate (ester) for carrying out the method.

Description

HERPES SIMPLEX TREATMENT
Technical Field
This invention relates to treatment of Herpes Simplex (Herpesvirus Hominis), a viral disease of widespread occurrence. Herpes Simplex occurs in two antigenic tyes. Herpes febrilis and Herpes genitalis, referred as Type 1 and Type 2. Infection is usually manifested by the appearance of vesicular eruptions, oral herpetic lesions, commonly referred to as fever blisters, or cold sores about the lips in the instance of Herpes Simplex Type 1, and vesicular lesions on and about the male or female genitalia in the instance of Herpes Simplex Type 2. Persons with Herpes Simplex infections are likely to have recurrent periods of lesion development spaced by periods of remission. Management of the condition involves easing the itching sensation which accompanies the lesion periods, and speeding remission. Background Art
While no cure is presently known for Herpes Simplex in either form, certain substances have been advanced for management of the disease. In U.S.P. 4,256,763 to McHugh a method of treating inflammatory viral infections such as Herpes Simplex and acne was
Figure imgf000003_0001
disclosed involving the application of 3,3-bis
(p-hydroxyphenyl) phthalide, in amounts up to 100 milligrams, preferably 15 to 30 milligrams initially and repetitively at predetermined intervals. Because 3,3-bis (p-hydroxyphenyl) phthalide is a cathartic, there is an unpleasant side effect to its use which suggests reduced usage concentrations, but the patentee does not suggest any lower dosage will be effective in Herpes Simplex management. Summary of the Invention
It is an object of the present invention to provide an effective Herpes Simplex treatment at much reduced dosage levels to minimize side effects. It is another object to provide a new use for phenol, 4,4'-(2-pyridinyl methylene) bis diacetate (ester). It is a further object to provide for the rapid amelioration of Herpes Simplex symptoms, itching, lesion development and the like, by treatment with quite low quantities of phenol, 4,4*-(2-pyridinyl methylene) bis diacetate (ester), and to maintain the patient in a remissive state with continued low dosage treatment after remission. Still other objects include provision of products comprising phenol, 4,4'- (2-pyridinyl methylene) bis diacetate (ester), carriers and therapeutic agents for coapplication with phenol, 4,4'-(2-pyridinyl methylene) bis diacetate (ester).
These and other objects of the invention to become apparent hereinafter, are realized in accordance with the invention in the method of treatment of Herpes Simplex infection condition which includes administering an effective dosage of phenol, 4,4'-(2-pyridinyl methylene) bis,- diacetate (ester) to a person having an Herpes Simplex condtion.
In particular embodiments, the method includes administering such dosage orally, administering a dosage of from about 0.1 to about 9.5 milligrams of phenol, 4,4'-(2-pyridinyl methylene) bis diacetate (ester), suspending the phenol, 4,4'-(2-pyridinyl methylene) bis,- diacetate (ester) in a carrier for administration, combining the phenol, 4,4'-(2-pyridinyl methylene) bis,- diacetate (ester) with a second therapeutic agent in an effective dosage for administration therewith, e.g. by selecting an effective dosage of one or more vitamins for coadministration with the phenol, 4,4'-(2-pyridinyl methylene) bis diacetate (ester), and carrier if any, and maintaining the phenol, 4,4'-(2-pyridinyl methylene) bis,- diacetate (ester) free of enteric coating for administration.
The invention further contemplates provision of a product comprising a dosage of phenol, 4,4'- (2-pyridinyl methylene) bis,- diacetate (ester) effective upon oral ingestion for management of Herpes Simplex, and less than is effective for catharsis of the person receiving the dosage and combined with an ingestible carrier. Typically, the product comprises a dosage between 0.1 and 9.5 milligrams, and may further comprise one or more vitamins in effective dosage, preferably free of an enteric coating.
OMPI Preferred Modes
Phenol, 4,4'-(2-pyridinyl methylene) bis diacetate (ester), commonly referred to as Bisacodyl, is a diphenyl trimethane suitably prepared from 2-pyridine- carboxaldehyde condensed with phenol in the presence of sulfuric acid or other dehydrant, followed by esterification with acetic anhydride and anhydrous sodium acetate, as described in U.S.P. 2,764,590. It is a white to off-white crystalline powder slightly soluble in water but fairly soluble in common organic solvents. It is known to be used as a contact laxative, acting to increase peristalsis throughout the large intestine. A typical dose as a laxative is oral or rectal not less than 10 milligrams and up to 30 milligrams and is administered in an enteric coating to ensure passage to the larage intestine. It is known to inhibit glucose absorption and intestinal Na-K-ATPase activity.
The effectiveness of phenol, 4,4'-(2-pyridinyl methylene) bis,- diacetate (ester) in treatment of Herpes Simplex is not to be expected from a study of its past usages or chemical structure, and is not scientifically explainable at this time. It has been found surprisingly effective in Herpes Simplex management, causing nearly immediate remission and suppressing recurrence, although administered at quite moderate levels, less than those recommended for laxative action, and far less than 3,3-bis (p- hydroyphenyl) phthalide dosages recommended in U.S.P. 4,256,763. The use of phenol, 4,4'-(2-pyridinyl methylene) bis,- diacetate (ester) as taught herein thus enables Herpes Simplex management with reduced
OMPI incidence of side effects than encountered with the use of alternate methodologies.
The phenol, 4,4'-(2-pyridinyl methylene) bis,- diacetate (ester) may be combined with other therapeutic agents each for its own purpose e.g. to relieve stress, or to enhance the effectiveness of the phenol, 4,4'-(2-pyridinyl methylene) bis,- diacetate (ester) when administered. Such agents as vitamins A, D, E, C, Folic acid, B-l, B-2, Niacin, B-6, and B-12, among others can be combined with the phenol, 4,4'-(2-pyridinyl methylene) bis diacetate (ester). Other agents for combining with phenol, 4,4'-{2-pyridinyl methylene) bis diacetate (ester) include amino acids, such as lysine and leucine; proteins such as gelatin and gliadin; or carbohydrates, e.g. starch, lactose and the like.
Whether administered orally, topically or intra¬ venously, the phenol, 4,4'-(2-pyridinyl methylene) bis,- diacetate (ester) may be suitably dispersed in a carrier, e.g. tablet or capsule carriers and components such as excipients, bulking agents, lubricants, disintegrants, dyes and the like as are known in tablet making technology for the purpose of easing the administration of the phenol, 4,4'-(2-pyridinyl methylene) bis diacetate (ester). The term carrier further embraces vehicles used or useful in preparing injection form of the phenol, 4,4 -(2-pyridinyl methylene) bis,- diacetate (ester) products of the invention, such as sesame oil and the like.
EXAMPLE I
Capsules of phenol, 4,4'-(2-ρyridinyl methylene) bis,- diacetate (ester) were prepared by mixing per
OMPI capsule 3.35 milligrams of phenol, 4,4'-(2-pyridinyl methylene) bis,- diacetate (ester) with 490 milligrams of an aliquot of a mixture of vitamins comprising:
Vitamin A 2500 units Vitamin D 400 units Vitamin E 15 units Vitamin C 60 mg. Folic acid 0.3 mg. Vitamin B-l 1.0 mg. Vitamin B-2 1.2 mg. Niacin 13.5 mg. Vitamin B-6 1.0 mg. Vitamin B-12 4.5 mg. blended with 2 parts of cornstarch per part of vitamin mix.
Adult males having a virulent recurrence of Herpes Simplex Types 1 and 2 were given a series of EXAMPLE I capsules prepared as above, or a like CONTROL I capsule prepared with phenolphthalein 3,3-bis (p-hydroxyphenyl phthalide) rather than phenol, 4,4'-(2-pyridinyl methylene) bis diacetate (ester), or a CONTROL II as taught in U.S.P. 4,256,763. The CONTROL II capsules comprised:
Phenolphthalein 30 mg.
Acetominophen 325 mg.
Chlorpheniramine
Maleate 2 mg.
Caffein 33 mg.
Phenylephrine HCL 10 mg.
The effective dosage rate for the CONTROL I and II treatments was 30 milligrams per 8 hours for the first day, and a like amount at 12 hour intervals
OMPI thereafter. The EXAMPLE I dosage rate was one capsule (3.35 mg. per dosage) every six to eight hours on the first day and thereafter at 8 to 12 hour intervals.
All subjects showed rapid remission. The EXAMPLE I material was no less effective for being at the reduced dosage rate, and incidence of diarrhea from the laxative effect was less of a problem than with the CONTROL I and II tests.
The inclusion of vitamins in the EXAMPLE I formulation adds stress relief factors to the formulation to ameliorate the stress which often accompanies onset of a Herpes condition.
EXAMPLE II A second capsule formula of the invention composition was prepared from: phenol, 4,4*-(2-pyridinyl methylene) bis diacetate (ester) 3 . 5 mg . phenacetin 350. mg . chloropheniramine maleate 3. mg . caffein 38. mg . phenylpropanolamine HCL 9. mg . by blending the ingredients eutectically.
EXAMPLE III
A tablet form of the invention dosage is prepared by blending phenol, 4,4-(2-pyridinyl methylene) bis diacetate (ester), 3.5 mg. , 100 mg. lactose, 100 mg. starch, and 10 mg. talc as a lubricant. It will be noted that this formulation can be packaged in capsule form with the omission of the talc and adjusting the lactose and starch concentration accordingly.
OMPI EXAMPLE IV
A protein containing capsule is prepared by blending eutectically phenol, 4,4'-(2-ρyridinyl methylene) bis diacetate (ester), 3.5 mg. , 200 mg. lactose, 100 mg. gliadin or gelatin protein, and about 100 mg. of the amino acid lysine.
EXAMPLE V
An intramuscular injectable formulation is prepared by blending, per dosage, 5 cc. sesame oil, 250 units of Vitamin E, and 5 mg. of phenol, 4,4'-(2-pyridinyl methylene) bis diacetate (ester).
-ξ R£Λ OMPI

Claims

1 WHAT IS CLAIMED IS:
1. A method for treating Herpes Simplex infection condition which includes administering an effective
5 dosage of phenol, 4,4'-(2-pyridinyl methylene) bis,- r diacetate (ester) for treating Herpex Simplex infection to a person having said condition.
2. The method according to claim 1, wherein said 10 effective dosage is administered orally.
3. The method according to claim 1 or 2, wherein said effective dosage is from about 0.1 to about 9.5 milligrams of phenol, 4,4'-(2-pyridinyl methylene)
15 bis,- diacetate (ester).
4. The method according to claim 1 wherein said phenol, 4,4'-(2-pyridinyl methylene) bis,- diacetate (ester) is suspended in a pharmaceutically acceptable
20 carrier for administration.
5. The method according to claim 1, wherein said phenol, 4,4*-(2-pyridinyl methylene) bis,- diacetate (ester) is combined with an effective dosage of a second
25 therapeutic agent.
6. The method according to claim 5 wherein such a second therapeutic agent is selected from the group consisting of one or more vitamins, amino acids,
30 carbohydrates, and proteins and mixtures thereof.
35
OMPI
7. The method according to claim 6 wherein said phenol, 4,4'-(2-pyridinyl methylene) bis,- diacetate (ester) is combined with a carrier for administration.
8. The method according to claim 1, wherein said phenol, 4,4'-(2-pyridinyl methylene) bis,- diacetate (ester) is maintained free of an enteric coating for administration.
9. A product free of an enteric coating comprising a dosage of phenol, 4,4'-(2-pyridinyl methylene) bis,- diacetate (ester) effective upon oral ingestion for treating Herpes Simplex infection.
10. The product according to claim 9 wherein said dosage of phenol, 4,4'-(2-pyridinyl methylene) bis,- diacetate (ester) is contained in a capsule.
11. The product according to claim 9 wherein said dosage of phenol, 4,4 '-(2-pyridinyl methylene) bis,- diacetate (ester) is less than is effective for catharsis of the persons receiving the dosage.
PCT/US1984/000920 1984-06-11 1984-06-11 Herpes simplex treatment WO1986000016A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP59502497A JPS61502395A (en) 1984-06-11 1984-06-11 Treatment of herpes simplex
EP19840902564 EP0183694A4 (en) 1984-06-11 1984-06-11 Herpes simplex treatment.
PCT/US1984/000920 WO1986000016A1 (en) 1984-06-11 1984-06-11 Herpes simplex treatment

Applications Claiming Priority (1)

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PCT/US1984/000920 WO1986000016A1 (en) 1984-06-11 1984-06-11 Herpes simplex treatment

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WO1986000016A1 true WO1986000016A1 (en) 1986-01-03

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Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2764590A (en) * 1952-03-17 1956-09-25 Thomae Gmbh Dr K Certain 4, 4'-disubstituted-diphenylpyridyl methanes and process
US2827465A (en) * 1958-03-18 Process of preparation of x
US3526635A (en) * 1968-12-03 1970-09-01 Synergistics Magnesium complex of dihydroxydiphenyl-isatin,4,4-dehydroxydiphenyl (2-pyridyl) methane,4,4'-dihydroxydiphenyl-2' - (aminophenyl methane) and phenophthalein
US4256763A (en) * 1978-09-19 1981-03-17 Mchugh John E Treatment of herpes simplex infections and acne

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2827465A (en) * 1958-03-18 Process of preparation of x
US2764590A (en) * 1952-03-17 1956-09-25 Thomae Gmbh Dr K Certain 4, 4'-disubstituted-diphenylpyridyl methanes and process
US3526635A (en) * 1968-12-03 1970-09-01 Synergistics Magnesium complex of dihydroxydiphenyl-isatin,4,4-dehydroxydiphenyl (2-pyridyl) methane,4,4'-dihydroxydiphenyl-2' - (aminophenyl methane) and phenophthalein
US4256763A (en) * 1978-09-19 1981-03-17 Mchugh John E Treatment of herpes simplex infections and acne

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
CHEMICAL ABSTRACTS, Vol. 88, No. 9, issued 27 February 1978 (Columbus, Ohio, USA), OHNUMA et al., Intestinal Absorption of Sodium Picosulfate and Bisacodyl 88:58209g (1978) *
CHEMICAl ABSTRACTS, Vol. 92, No. 5, issued 4 February 1980 (Columbus, Ohio, USA), STEINBACH et al., Studies Under Dosage Precision of Bisacodyl in Oral Laxatives 92:47265 (1980) *
See also references of EP0183694A4 *

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EP0183694A1 (en) 1986-06-11
EP0183694A4 (en) 1987-06-16

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