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- Nxera doubles down on obesity drugs as Pfizer, Novo and Terns exit GLP-1 candidates
Nxera doubles down on obesity drugs as Pfizer, Novo and Terns exit GLP-1 candidates
On the same day Pfizer, Novo Nordisk and Terns scrapped GLP-1 drugs, Nxera Pharma announced a bold new pipeline of seven obesity-focused therapies, headlined by a proprietary oral GLP-1 agonist.
Backstory: Nxera, formerly Sosei Heptares, helped pioneer GLP-1 receptor structure mapping and had co-developed the now-discontinued PF-06954522 with Pfizer. The candidate was pulled due to portfolio priorities, not safety, following Pfizer’s prior GLP-1 setbacks tied to liver issues. Pfizer now relies on a single phase 2 GIPR antagonist and is exploring external opportunities to rebuild its position in the competitive obesity market.
Zoom in: Nxera’s new obesity program is independent of its prior collaborations with Pfizer and Eli Lilly. It includes GLP-1, GIP, Apelin, and Amylin receptor agonists, a GIP antagonist, and two undisclosed long-acting treatments.
Big picture: Pfizer is not the only big pharma to trim its obesity portfolio, as Novo Nordisk also dropped multiple obesity and metabolic disease drug candidates as part of a major pipeline overhaul linked to underwhelming obesity drug sales and executive departures.
Despite positive phase 2 weight-loss results, the GLP-1/GIP co-agonist NNC0519-0130 was discontinued due to “portfolio considerations,” alongside the CB1 receptor blocker INV-347, which was safe but had unfavorable pharmacokinetics.
Additionally, the development of zalfermin for liver fibrosis was halted after limited efficacy. The drug ANGPTL3i for dyslipidemia was also shelved due to strategic reprioritization.
Not the only ones: Terns Pharmaceuticals also announced it will cease funding clinical development of its metabolic disease programs by the end of 2025, shifting focus to its oncology asset, TERN-701, for chronic myeloid leukemia.
The company plans to seek partners for its metabolic pipeline, which includes TERN-601, an oral GLP-1 receptor agonist in a phase 2 obesity trial, and two earlier-stage candidates: TERN-501 for NASH and the TERN-800 series targeting GIPR.
Yes, but: Citing the high costs and competitive landscape in obesity treatment, Terns believes larger pharmaceutical partners are better positioned to advance these programs through late-stage development and commercialization. Of course, this assumes that they stop abandoning their own pipelines first!