Peptide News Digest

#Bardet-Biedl-Syndrome

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Industry · View digest

Superluminal Medicines Raises Oversubscribed $60 Million Series B to Advance Selective MC4R Agonist Into Phase 1 for Rare Genetic Obesity and Hypothalamic Obesity

Superluminal Medicines announced Thursday September 3, 2026 an oversubscribed $60 million Series B financing round led by BVF Partners with participation from Deep Track Capital, Perceptive Advisors, RA Capital Management, Insight Partners, NVIDIA, Catalio Capital Management, Eli Lilly and Company, Cooley, and Gaingels. Proceeds will advance the company's lead clinical program (a selective, biased MC4R agonist) into Phase 1 for rare genetic forms of obesity including Bardet-Biedl syndrome (BBS) and hypothalamic obesity, targeting Phase 1 initiation by end of 2026. Superluminal's technology platform uses AI plus GPCR-structural chemistry to design biased agonists with reduced off-target signaling. The MC4R agonist positioning is directly against Rhythm Pharmaceuticals's Imcivree (setmelanotide, the currently-approved MC4R agonist peptide for BBS and hypothalamic obesity) — a small-molecule alternative would have oral bioavailability advantages plus different tolerability profile. Eli Lilly's investor participation extends Lilly's obesity-adjacent equity portfolio.

Clinical Trials · View digest

Rhythm Pharmaceuticals Presents Setmelanotide ENDO 2026 Data Across Three Rare-Disease Indications: Acquired Hypothalamic Obesity 2.5-Year LTE, Prader-Willi Syndrome Phase 2 Interim, and Bardet-Biedl Syndrome Real-World

Rhythm Pharmaceuticals (Nasdaq: RYTM) presented seven setmelanotide abstracts at ENDO 2026 covering three rare-disease patient populations. Christian Roth (Seattle Children's) reported 2.5-year Phase 2 + long-term extension data in acquired hypothalamic obesity showing -18.9% mean BMI reduction across all 11 participants. The PWS interim Phase 2 (June 13) reported across 17 patients (10 adult, 7 pediatric) showed 3.11% mean BMI reduction in adults and 3.00% in pediatric patients, with 8 of 10 baseline-hyperphagic patients hitting a 7-point HQ-CT reduction, and 4.19% fat-mass loss with 0.74% lean-mass gain across 16 DEXA evaluations. Two BBS late-breaking posters from Caroline Huber covered real-world hyperphagia and healthcare-utilization outcomes from the 6-month RESTORE study. All three indications reinforce the MC4R-agonist rationale for Phase 3.