Wednesday 9 July 2025
  • About
  • Contact
  • Login
  • VC & Investment
  • M&A
  • AI
  • Podcasts
  • News
    • Pharmaceutical News
    • Biotechnology News
    • Generics News
    • Biosimilars news
    • In Brief
    • Legal
    • Company Pages
    • In The Boardroom
  • Insights
    • Analysis
    • Special Report
    • Interviews
    • Expert View
    • From Our Correspondent
    • One To Watch Companies
    • Digital Pharma
    • Pharma Leaders
  • Regulatory
    • FDA
    • EMA
    • Pricing, Reimbursement and Access
    • Regulation
    • Government Affairs
    • Trump Administration
  • Therapy Areas
    • Dermatologicals
    • Oncology
    • Neurological
    • Rare Diseases
    • Hematology
    • Cardio Vascular
    • Diabetes
    • Cell And Gene Therapy
  • Conferences
    • JPM Healthcare Conference
    • ESMO
    • ASCO
    • ASH
    • EULAR
    • AAIC
    • EASD
    • Forthcoming Events
  • Ones to Watch
  • About
  • Contact
  • Newsletter
  • Sign inSubscribe
Subscribe
  • Home
  • Octreotide for AIDS-Related Diarrhea

Octreotide for AIDS-Related Diarrhea

10 September 1995

A multicenter study of Sandoz' somatostatin analog octreotide for the treatment of AIDS-related diarrhea has produced mixed results, according to a report in AIDS Clinical Care.

Around 130 AIDS patients were given octreotide or placebo by subcutaneous injection three times a day. After 21 days, 46% of the octreotide group had achieved the goal of a 30% decrease in stool weight, compared to 36% of the placebo group. The two groups had similar reductions in bowel-movement frequency, according to the report.

Although patients with idiopathic diarrhea (diarrhea lasting more than 13 weeks, body weight under 60 kg, or CD4 levels below 50) showed a better response to the treatment, the differences between the two groups remained insignificant. During a subsequent open-label phase, the octreotide dose was boosted, and after eight weeks, both stool weight and bowel-movement frequency decreased significantly. The researchers note that even though the results of the controlled study were disappointing, the open-label results indicate that longer-term treatment at higher doses could be effective.

This article is accessible to registered users, to continue reading please register for free.  A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.

Login to your account

Try before you buy

 

Free

7 day trial access

Take a Free Trial
  • All the news that moves the needle in pharma and biotech
  • Exclusive features, podcasts, interviews, data analyses and commentary from our global network of life sciences reporters.
  • Receive The Pharma Letter daily news bulletin, free forever.

Become a subscriber

 

£820

Or £77 per month

Subscribe Now
  • Unfettered access to industry-leading news, commentary and analysis in pharma and biotech.
  • Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results.
  • Daily roundup of key events in pharma and biotech.
  • Monthly in-depth briefings on Boardroom appointments and M&A news.
  • Choose from a cost-effective annual package or a flexible monthly subscription
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed

Chairman, Sanofi Aventis UK





More ones to watch >


Sign up to receive email updates
Join industry leaders for a daily roundup of biotech & pharma news

Today's issue

Phesi flags mounting risks for phase III atopic dermatitis trials
Pharmaceutical
Phesi flags mounting risks for phase III atopic dermatitis trials
9 July 2025
Pharmaceutical
Novo files for EMA approval of higher-dose Wegovy as Indian market heats up
9 July 2025
Biotechnology
Actithera raises $75.5 million in Series A financing
9 July 2025
Pharmaceutical
Trump ramps up threat of steep tariffs on drug imports
9 July 2025
Biotechnology
Crescent brings in Jan Pinkas as CSO
8 July 2025
Biotechnology
Centauri opts for experience with CMO appointment
8 July 2025
Biotechnology
Centivax raises $45 million to launch universal flu vaccine into clinic
8 July 2025

Company Spotlight

A late-stage clinical biotechnology company pioneering physics-based therapeutic approaches to treatments.






The Pharma Letter

39-43 Putney High Street, Putney
London, SW15 1SP
United Kingdom

  • About us
  • Contact
  • Subscribe
  • Sponsorship/advertising


  • Terms and Conditions
  • Privacy Policy
  • Twitter
  • Linkedin

Copyright © The Pharma Letter 2025   |   Headless Content Management with Blaze