Biohaven Oral Presentation at ASN Kidney Week 2026 Spotlights BHV-1420, a Novel TRAP Degrader Designed to Selectively Remove the Autoantibodies that Drive Membranous Nephropathy
Biohaven Presents Preclinical Data For BHV-1420 At American Society Of Nephrology Kidney Week 2026
Biohaven Could Transform With Troriluzole's FDA Approval, RBC Says
Why Biohaven (BHVN) Is Up 25.0% And What's Next After FDA Review Acceptance
RBC Capital Maintains Sector Perform on Biohaven, Raises Price Target to $22
Biohaven (BHVN) Soars 25% on FDA Drug Review, Price Target Upgrade
Why Biohaven Catapulted 25% — And Why It Might Not Be Done Sprinting
Biohaven Stock Heads for Best Day in 3 Years as FDA Agrees to Review Drug Again
Biohaven’s previously rejected rare disease drug to get fresh FDA review
BHVN Stock Eyes Biggest Single-Day Gain In 4 Years After FDA Approval For Vyglxia
Biohaven stock surges 25% on FDA acceptance of drug filing
Biohaven Rebounds With FDA Review Date for Rare Disease Drug
Biohaven partners with Ono in $100m IgG degrader deal
Biohaven Expands Asian Licensing Footprint Through Strategic Ono Agreement
Biohaven Enters Strategic Licensing Agreement with Ono Pharma for Extracellular IgG Degraders in Japan and Select Asian Regions, Lead Candidate BHV-1300 in Phase 3 for Graves' Disease
Biohaven Licenses MoDE IgG Degraders To Ono For Japan, South Korea, Taiwan And ASEAN For Up To $100M Near-Term Payments Including $80M Upfront; BHV-1300 In Phase 3 For Graves' Disease
Biohaven To Present Data On BHV-1530, FGFR3-Directed ADC Using Topoisomerase I Payload, At 38th EORTC-NCI-AACR Symposium On Molecular Targets And Cancer Therapeutics
Has Biohaven (BHVN) Fallen Far Enough to Look Fully Priced?
Xenon Stock Craters on Drug Trial Setback. Its Failure Could Be This Rival’s Gain.
Biohaven’s epilepsy drug hit with FDA clinical hold
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