EloraTZP vs Retatrutide: What the Three Datasets Show
A Lilly slide shows 29% weight loss in 31 weeks with eloralintide plus tirzepatide. Only 3 of 12 had data, and it can’t be compared with retatrutide’s 28.3%.
A Lilly slide shows 29% weight loss in 31 weeks with eloralintide plus tirzepatide. Only 3 of 12 had data, and it can’t be compared with retatrutide’s 28.3%.
Novo signed with Orbis for up to $1.4bn on oral macrocycles. Against two 2026 approvals, what the deal establishes and what it does not.
Three 2026 recalls traced to one contaminated raw material show why chemical purity and biological contamination are different questions.
The TGA tested a vial sold as retatrutide after a hospitalisation: no retatrutide, and about eight times the semaglutide of registered products.
WADA named flmodafinil and fladrafinil under class S6 in 2026. Why it adds examples rather than a new ban, and what it means for confirmatory analysis.
Samsung Biologics opened a CHF 1.46 billion tender for PolyPeptide on 15 September, with 55.65% of shares already committed. CordenPharma closed its AmbioPharm acquisition in August. The scarce asset is not synthesis, it is purification.
An FT Lex column put potential US peptide sales near $80bn a year. Analysts quoted by Reuters put the market regulatory change would unlock at $2.2 to $3.3bn. Both are right, because they measure different things. The arithmetic behind each.
TwoStep Therapeutics cleared an IND for TS-104, a peptide-drug conjugate delivering MMAE through an integrin-binding peptide, alongside a $62.5m Series A. What PDCs change relative to antibody-drug conjugates, and what the public record does not yet say.
Novo Nordisk reported that 40.4% of children aged 6 to 11 fell below the obesity threshold on semaglutide against 0% on placebo. What that figure measures, why it is a secondary endpoint, how paediatric BMI thresholds work, and what the announcement did not report.
A Phase 1 study of BPC-157 after arthroscopic rotator cuff repair was posted to ClinicalTrials.gov on 3 September 2026. It is not the first registered human study, it states no dose, and it registers one endpoint. A close reading of the record.
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