News about "Neurocrine Biosciences"

Neurocrine Initiates First-in-Human Trial for Novel Obesity Therapy NBIP-2118

Neurocrine Initiates First-in-Human Trial for Novel Obesity Therapy NBIP-2118

Neurocrine launches phase I trial of NBIP-2118, a novel CRF2 agonist aimed at delivering fat-specific weight loss while preserving muscle in obesity treatment.

Neurocrine Biosciences | 05/05/2026 | By News Bureau

Neurocrine Biosciences to Acquire Soleno Therapeutics in USD 2.9 Billion Deal

Neurocrine Biosciences to Acquire Soleno Therapeutics in USD 2.9 Billion Deal

The acquisition brings first-in-class Prader-Willi syndrome therapy VYKAT XR into Neurocrine’s portfolio, strengthening its position in endocrinology and rare diseases.

Neurocrine Biosciences | 07/04/2026 | By News Bureau

Neurocrine to Acquire Soleno Therapeutics

Neurocrine to Acquire Soleno Therapeutics

Neurocrine to acquire Soleno Therapeutics, adding US FDA-approved VYKAT XR for Prader-Willi Syndrome and strengthening its rare disease and endocrinology portfolio.

Neurocrine Biosciences | 07/04/2026 | By News Bureau

Dr. Sanjay Keswani to Lead Medical Strategy at Neurocrine Biosciences as New CMO

Dr. Sanjay Keswani to Lead Medical Strategy at Neurocrine Biosciences as New CMO

Dr. Keswani, who has more than 20 years of pharmaceutical industry experience with broad R&D expertise in multiple therapeutic areas, will lead the clinical development and medical affairs activities at Neurocrine.

Neurocrine Biosciences | 05/04/2025 | By Abha 394

Neurocrine Biosciences Secures FDA Approval of CRENESSITY

Neurocrine Biosciences Secures FDA Approval of CRENESSITY

CRENESSITY, a potent and selective oral corticotropin-releasing factor type 1 receptor (CRF1) antagonist, is the first and only classic CAH treatment that directly reduces excess adrenocorticotropic hormone (ACTH) and downstream adrenal androgen production, allowing for glucocorticoid dose reduction.

Neurocrine Biosciences | 16/12/2024 | By Aishwarya 208

Nxera Pharma to Get USD 35 Million from Neurocrine for Phase 2 Trial with NBI- '568

Nxera Pharma to Get USD 35 Million from Neurocrine for Phase 2 Trial with NBI- '568

The NBI-’568-SCZ2028 dose-finding study met its primary endpoint for the once-daily 20 mg dose and was generally safe and well tolerated at all doses studied, supporting Neurocrine’s intentions to advance NBI- ‘568 into Phase 3 clinical trials in early 2025.

Neurocrine Biosciences | 03/09/2024 | By Aishwarya 353


 

 

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