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LPAR1 antagonist

PharmaDeviceNews LPAR1 antagonist

Pharma & Biotech

Contineum Therapeutics paper sharpens PIPE-791 case, but Phase 2 IPF data remain decisive

by Pallavi Madhiraju
July 1, 2026
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Discover why Contineum Therapeutics’ PIPE-791 paper strengthens the LPAR1 case while Phase 2 IPF data remain the decisive clinical test.

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Niagen Bioscience’s NB4168 has secured U.S. FDA Rare Pediatric Disease and European orphan designations as the company advances the experimental ataxia telangiectasia therapy toward human trials. Representative image.

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Representative image of biopharma laboratory research. Gilead Sciences and Merck’s latest Phase 3 updates highlight the promise of once-weekly HIV treatment with islatravir and lenacapavir, while raising fresh questions over Trodelvy’s lung cancer expansion strategy.

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biologics clinical trials Eli Lilly and Company European Medicines Agency FDA FDA approval immuno-oncology immunotherapy Inc. medical devices oncology precision oncology rare disease U.S. Food and Drug Administration United States Food and Drug Administration

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