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News & Analysis

Research-peptide news, regulatory updates, and industry analysis.

What changed and why it matters. Regulatory shifts, new research, vendor and market moves — written for researchers. Articles are AI-researched and editorially reviewed, and are provided for research and educational purposes only.

Topic
Research

Roche reports positive Phase II results for petrelintide in obesity: amylin analog advances to late-stage trials

Roche's amylin analog petrelintide shows promising weight loss in Phase II, positioning it alongside cagrilintide as next-generation amylin-based therapeutics move toward the clinic.

1 July 20264 min read
01
Research

Ecnoglutide Phase 3 results published in The Lancet: biased GLP-1 receptor agonist shows significant weight loss in obesity trial

A multicentre randomised Phase 3 trial of ecnoglutide, published in The Lancet, demonstrates the potential of biased GLP-1 receptor agonism as a differentiated approach to obesity treatment.

1 July 20265 min read
02
Research

VK2735 Phase 2 VENTURE trial: Viking Therapeutics' dual GIP/GLP-1 agonist shows up to 14.7% weight loss in 13-week study

The Phase 2 VENTURE trial of VK2735, a subcutaneous dual GIP/GLP-1 receptor agonist from Viking Therapeutics, demonstrated dose-dependent weight loss of up to 14.7% at 13 weeks in adults with obesity. Results were published in a peer-reviewed PubMed-indexed journal, adding to the growing body of evidence for next-generation multi-receptor agonists in obesity treatment.

1 July 20264 min read
03
Regulatory

NICE recommends tirzepatide (Mounjaro) for obesity on the NHS: what researchers need to know about TA1026

NICE TA1026: tirzepatide for obesity — eligibility, review points, and what this UK regulatory milestone means for peptide research.

1 July 20265 min read
04
Safety

MHRA warns of pulmonary aspiration risk with GLP-1 and dual GIP/GLP-1 receptor agonists before anaesthesia

UK regulator strengthens guidance on GLP-1 agonists and anaesthesia: what peptide researchers need to know about delayed gastric emptying and aspiration risk.

1 July 20264 min read
05
Safety

MHRA warns of very rare NAION risk with semaglutide: UK regulator adds vision-loss precautions to Wegovy, Ozempic and Rybelsus

The UK MHRA has published a Drug Safety Update warning that semaglutide may very rarely be associated with non-arteritic anterior ischaemic optic neuropathy (NAION), a condition that can cause sudden vision loss. The EMA's pharmacovigilance committee is also reviewing the signal.

1 July 20264 min read
06
Regulatory

FDA Pharmacy Compounding Advisory Committee to review BPC-157, TB-500 and thymosin peptides: what peptide researchers need to know

The US FDA's PCAC will evaluate whether BPC-157, TB-500, thymosin alpha-1 and other popular research peptides remain on the 503A bulk substances list — a decision that could reshape the global research peptide supply chain

1 July 20266 min read
07
Regulatory

FDA clarifies compounding policy as GLP-1 shortage formally resolves: what it means for peptide researchers

With the FDA declaring an end to the semaglutide and tirzepatide shortages, compounding pharmacies must cease production. The policy shift has ripple effects for the broader research peptide market.

1 July 20266 min read
08
Regulatory

FDA requests removal of suicidal ideation boxed warning from GLP-1 receptor agonists

After a multi-year review, the US FDA concluded there is no causal link between GLP-1 receptor agonists and suicidal thoughts or behaviours, and has asked manufacturers to remove the boxed warning.

1 July 20265 min read
09
Research

Danuglipron Phase 2b results published: Pfizer's oral GLP-1 shows up to 12.9% weight loss but high discontinuation rates

Pfizer's oral small-molecule GLP-1 receptor agonist danuglipron demonstrated dose-dependent weight loss up to 12.9% in a Phase 2b trial, but nearly 38% of participants discontinued due to adverse events.

1 July 20265 min read
10
Research

CagriSema REDEFINE-1 results: Novo Nordisk's dual amylin/GLP-1 combination achieves 22.7% weight loss in Phase 3

Novo Nordisk's CagriSema (cagrilintide + semaglutide) delivered a 22.7% mean weight reduction in the REDEFINE-1 Phase 3 trial, but fell short of expectations for superiority over semaglutide alone.

1 July 20265 min read
11
Research

SURMOUNT-5: Tirzepatide outperforms semaglutide in first head-to-head obesity trial published in NEJM

Eli Lilly's dual GIP/GLP-1 agonist tirzepatide demonstrated superior weight loss compared to semaglutide in the landmark direct-comparison SURMOUNT-5 trial, results published in the New England Journal of Medicine.

1 July 20264 min read
12
Research

Retatrutide Phase 3 TRIUMPH-1 results: Eli Lilly's triple-agonist delivers powerful weight loss in pivotal obesity trial

Eli Lilly has announced top-line results from the first pivotal Phase 3 trial of retatrutide, a GLP-1/GIP/glucagon triple agonist, in adults with obesity. The drug's mechanism — targeting three incretin pathways simultaneously — positions it as a potential next-generation therapy beyond tirzepatide.

1 July 20264 min read
13
Research

MariTide Phase 2 obesity data presented at ADA 2025: monthly GIP/GLP-1 antagonist-agonist shows sustained weight loss

Amgen's MariTide (maridebart cafraglutide) demonstrated up to 20% weight loss at 52 weeks in a Phase 2 obesity trial, with a durable monthly dosing profile.

30 June 20264 min read
14
Research

Pemvidutide Phase 2b MASH results published in The Lancet: dual GLP-1/glucagon agonist shows fibrosis improvement

The GLP-1/glucagon dual agonist pemvidutide met its primary endpoint in a Phase 2b trial for metabolic dysfunction-associated steatohepatitis, published in The Lancet.

30 June 20264 min read
15
ResearchFeatured

Orforglipron Phase 3 ACHIEVE-1 results published in NEJM: oral GLP-1 agonist matches injectable weight loss

The first Phase 3 data for an oral GLP-1 receptor agonist show 12–15% weight loss at 36 weeks, positioning orforglipron as a potential tablet alternative to injectable semaglutide and tirzepatide.

30 June 20264 min read
16
RegulatoryFeatured

MHRA tightens guidance on research-peptide labelling

New wording clarifies that "not for human consumption" must appear on the primary label, not just the certificate.

30 June 20263 min read
17