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Peptide Therapy News

Regulatory Research

Source review through · Event dates appear with reports

The documents behind the dates

The original notices, labels and papers, with a few words on what each tells you.

Reading the records

Peptide Therapy News links to the records behind its reports. This page collects them, with a note on what each explains. The links open the original page or PDF, so you can check the details in context.

The publication’s source-review cutoff is 27 October 2026. Dates below identify the announcement, document or source update. An old announcement can explain a past decision without answering what happened later.

The source desk

Step 3: Clinical Research

FDA · checked 27 October 2026

Explains what phase 2 testing can tell researchers, and why more testing follows.

National supply and the rules for compounded copies

FDA · updates through 1 April 2026

Tracks the shortage decisions and grace periods for compounded copies, medicines prepared outside approved finished-product manufacturing.

FDA’s two-table account of peptide nominations

FDA · snapshot current as of 22 April 2026

Shows Category 2 and withdrawn requests in separate tables. Withdrawal does not mean safety clearance.

FDA’s safety concerns about unapproved medicines

FDA · checked 27 October 2026

Explains why compounded medicines are not FDA-approved and why retatrutide cannot be compounded under federal law.

American Diabetes Association highlights retatrutide phase 2 findings

American Diabetes Association · 26 June 2023 · PDF

Announces two mid-stage retatrutide studies: one in adults with type 2 diabetes, one in adults without it.

Retatrutide obesity trial: the original paper

New England Journal of Medicine · 2023

Reports weight loss and side effects, including stomach problems and a faster heartbeat, in adults without type 2 diabetes.

Retatrutide diabetes trial: the original paper

The Lancet · 2023

Reports blood-sugar and weight findings in adults with type 2 diabetes. This was a different study from the obesity trial.

The March 2024 semaglutide cardiovascular decision

FDA · 8 March 2024

Sets out the heart-risk approval for semaglutide, sold as Wegovy, and the adults it covers.

Wegovy (semaglutide) prescribing information

National Library of Medicine, DailyMed · checked 27 October 2026

Gives semaglutide’s warnings and the trial evidence behind the heart-risk approval.

Drug reverses signs of liver disease in people living with HIV

National Institutes of Health · 15 October 2019

Announces the year-long tesamorelin study that found lower liver fat in adults living with HIV.

Effects of tesamorelin on non-alcoholic fatty liver disease in HIV

The Lancet HIV · 2019

Reports the liver-fat findings in adults with HIV and fatty liver disease.

Original Egrifta (tesamorelin) approval letter

FDA · 10 November 2010 · PDF

Records tesamorelin’s original approval for excess abdominal fat in HIV-associated lipodystrophy, a change in body-fat distribution.

Egrifta WR (tesamorelin) supplement approval letter

FDA · 25 March 2025 · PDF

Approves a new tesamorelin formulation and multiple-dose presentation. It is not a general weight-loss approval.

Egrifta WR (tesamorelin) prescribing information

National Library of Medicine, DailyMed · checked 27 October 2026

Specifies adults, rules out a general weight-loss use, and explains warnings about blood sugar, fluid retention and raised growth-factor levels.