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They also slow down the digestion of food and increase the feeling of fullness after eating. Moving forward, the company will continue advancing the clinical program for danuglipron (PF-06882961), subject to results from the Phase 2 study C3991004 (NCT05579977). These medicines are intended to keep blood sugar at healthy levels and work by increasing the amount of glucagon released into the blood. NYSE: PFE) today announced its decision to continue advancing the clinical program for danuglipron (PF-06882961), subject to results from the Phase 2 study C3991004 (NCT05579977). Both danuglipron index.php?rest_route=/oembed/1.0/embed and lotiglipron (PF-07081532) are experimental medicines that are not approved for use by health authorities at this time.

About Danuglipron and Lotiglipron Danuglipron (PF-06882961) and lotiglipron (PF-07081532) are experimental medicines that are not approved for use by health authorities at this time. NYSE: PFE) today announced its decision to continue to progress one oral late-stage glucagon-like peptide-1 receptor agonist (GLP-1-RA) candidate toward further clinical development for the danuglipron program. The Phase 2b study of danuglipron to date, including transaminase changes, appears to be discontinued NEW YORK-(BUSINESS WIRE)- Pfizer Inc. D, Senior Vice President and Chief Scientific Officer, Internal Medicine, Pfizer. NYSE: PFE) today announced its decision to index.php?rest_route=/oembed/1.0/embed continue to progress one oral late-stage glucagon-like peptide-1 receptor agonist (GLP-1-RA) candidate toward further clinical studies.

Moving forward, the company will continue advancing the clinical development for the danuglipron program. GLP-1RA program and its investigational GLP-1 receptor agonist, danuglipron, including their potential benefits, potential profile, an ongoing Phase 2 study C3991004 (NCT05579977). About Danuglipron and Lotiglipron Danuglipron (PF-06882961) and lotiglipron (PF-07081532) are experimental medicines that are not approved for use by health authorities at this time. NCT05788328) and laboratory measurements of elevated transaminases in these Phase 1 studies as well as the ongoing Phase 2 study C3991004 (NCT05579977). The company expects to finalize plans index.php?rest_route=/oembed/1.0/embed for the danuglipron program.

Pfizer assumes no obligation to update forward-looking statements contained in this release is as of June 26, 2023. The most common adverse events were nausea, vomiting and diarrhea. The safety profile of danuglipron in non-diabetic obesity participants is currently ongoing (doses ranging from 2. L; and body weight of -4. Both danuglipron and lotiglipron are taken as a tablet by mouth and are a type of medicine known as GLP-1-RA.