clinical trial results

42 articles
GlobeNewswire Inc.GlobeNewswire Inc.··Rosen Law Firm

Aldeyra Therapeutics Faces Securities Lawsuit Over Reproxalap Trial Claims

Rosen Law Firm sues Aldeyra Therapeutics for false reproxalap trial claims. Lead plaintiff deadline: May 29, 2026.
ALDXsecurities class actionmisleading statements
GlobeNewswire Inc.GlobeNewswire Inc.··Bronstein, Gewirtz & Grossman Llc

Aldeyra Faces Class Action Over Reproxalap Trial Data Misstatements

Class action filed against $ALDYA alleging false statements about reproxalap trial results. Eligible investors covered Nov 2023-Mar 2026.
ALDXsecurities fraudclass action lawsuit
GlobeNewswire Inc.GlobeNewswire Inc.··Rosen Law Firm

Aldeyra Faces Securities Lawsuit Over Reproxalap Trial Data; May 29 Deadline Looms

Rosen Law Firm files class action against $ALDX over allegedly misleading reproxalap clinical trial statements. Lead plaintiff deadline: May 29, 2026.
ALDXsecurities fraudclass action lawsuit
GlobeNewswire Inc.GlobeNewswire Inc.··Bronstein, Gewirtz & Grossman Llc

Aldeyra Faces Class Action Over Reproxalap Trial Claims; Investors Urged to Join Suit

Class action filed against Aldeyra Therapeutics alleging false reproxalap trial data claims; investors from Nov 2023-Mar 2026 may be eligible.
ALDXsecurities fraudclass action lawsuit
GlobeNewswire Inc.GlobeNewswire Inc.··Johnson Fistel, Pllp

Johnson Fistel Investigates Viridian Therapeutics Over Phase 3 Trial Disclosure

Johnson Fistel investigates Viridian Therapeutics for potential securities law violations related to Phase 3 REVEAL-1 trial disclosures, offering shareholders potential loss recovery options.
VRDNBAKTATTsecurities fraudinvestor losses
BenzingaBenzinga··Vandana Singh

Biogen Stock Surges on FDA Nod for High-Dose Spinraza in Rare Muscle Disease

$BIOG rallies as FDA approves high-dose Spinraza for spinal muscular atrophy, while litifilimab shows positive Phase 2 lupus results.
BIIBFDA approvalbiotech
BenzingaBenzinga··Vandana Singh

Boston Scientific Plunges 9% on Trial Win Paradox as Growth Concerns Overshadow Data

$BSX shares dropped 9.02% to 52-week lows despite positive WATCHMAN FLX and EKOS trial results, signaling investor caution amid broader growth concerns.
BSXclinical trial resultsmedical devices
GlobeNewswire Inc.GlobeNewswire Inc.··Novartis

Novartis Fabhalta Shows 49% Slowing of Kidney Decline in Landmark IgAN Study

Novartis' Fabhalta slowed kidney function decline by 49.3% in Phase III trial, with FDA priority review granted for IgA nephropathy treatment.
NVSFDA approvalkidney disease
GlobeNewswire Inc.GlobeNewswire Inc.··Priovant Therapeutics / Roivant Sciences

Priovant's Brepocitinib Clears Phase 3 Trial for Rare Muscle Disease, Eyes 2026 FDA Approval

Priovant's brepocitinib met Phase 3 endpoints for dermatomyositis treatment, earning FDA Priority Review with Q3 2026 decision expected.
ROIVclinical trial resultsautoimmune disease
GlobeNewswire Inc.GlobeNewswire Inc.··Na

Biogen's Lupus Drug Shows Promise Again, Edges Closer to Historic FDA Approval

Biogen announces second positive Phase 2 trial of litifilimab for cutaneous lupus, showing 11.8% greater disease reduction than placebo, advancing toward potential first targeted CLE therapy in 70 years.
BIIBFDA Breakthrough Therapy Designationclinical trial results
The Motley FoolThe Motley Fool··Prosper Junior Bakiny

Two Biotech Stocks Poised to Outpace Summit Therapeutics Amid FDA Uncertainty

Summit Therapeutics faces FDA decision on ivonescimab by November 2026 amid efficacy concerns, while Axsome and Madrigal positioned for outperformance.
AXSMMDGLSMMTregulatory riskFDA approval
GlobeNewswire Inc.GlobeNewswire Inc.··Aclaris Therapeutics, Inc.

Aclaris to Present Phase 2a ATI-2138 Data at 2026 AAD Meeting

Aclaris Therapeutics will present previously unreported Phase 2a trial results for ATI-2138, an oral dual ITK/JAK3 inhibitor, at the 2026 AAD Annual Meeting in Denver.
ACRSclinical trial resultsatopic dermatitis
BenzingaBenzinga··Vandana Singh

Eli Lilly's Eczema Drug Clears Phase 3 Pediatric Hurdle, Eyes Label Expansion

Eli Lilly's Ebglyss shows strong efficacy in pediatric atopic dermatitis trial, with 63% achieving significant skin clearance. Company plans regulatory submission for label update.
LLYFDA approvalPhase 3 trial
GlobeNewswire Inc.GlobeNewswire Inc.··Holzer & Holzer, Llc

Four Companies Face Shareholder Lawsuits Over Alleged Disclosure Failures

Four companies face April 6, 2026 lead plaintiff deadline in shareholder lawsuits alleging disclosure violations involving valuations, clinical trials, and fraudulent promotion.
TCPCMREORAREPOMsecurities fraudclass action lawsuit
GlobeNewswire Inc.GlobeNewswire Inc.··Pmv Pharmaceuticals, Inc.

PMV Pharma's Rezatapopt Shows Promise, But Cash Clock Ticks Toward 2027

PMV Pharmaceuticals reports 50% response rate for ovarian cancer drug rezatapopt, but faces funding pressure with cash runway extending only to Q2 2027.
PMVPclinical trial resultsorphan drug designation
BenzingaBenzinga··Vandana Singh

Roche's Obesity Drug Falls Short of GLP-1 Rivals in Phase 2 Results

Roche's obesity drug petrelintide achieved 10.7% weight loss in Phase 2 trials but significantly trails GLP-1 rivals Novo Nordisk and Eli Lilly, triggering sharp stock declines.
LLYNVORHHBYclinical trial resultsweight loss
GlobeNewswire Inc.GlobeNewswire Inc.··Dbv Technologies

DBV Technologies' Peanut Allergy Patch Shows Strong Phase 3 Data Ahead of FDA Submission

DBV Technologies announced strong Phase 3 data for VIASKIN® Peanut patch, with 82.8% of treated children showing improved tolerance. FDA submission planned for H1 2026.
DBVTFDA approvalclinical trial results
BenzingaBenzinga··Vandana Singh

Bristol Myers' Experimental Breast Cancer Treatment Demonstrates Survival Gains in Advanced Patients

Bristol Myers Squibb's experimental breast cancer drug showed survival improvements in advanced patients, though stock declined slightly following the announcement.
BMYCELGrbreast cancerPhase 3 trial
GlobeNewswire Inc.GlobeNewswire Inc.··Argenx Se

argenx's VYVGART Meets Primary Endpoint in Ocular Myasthenia Gravis Trial

argenx's VYVGART met its primary endpoint in a Phase 3 ocular myasthenia gravis trial, showing significant symptom improvements. The company plans FDA approval for label expansion.
ARGXFDA approvalPhase 3 trial
GlobeNewswire Inc.GlobeNewswire Inc.··Na

Fulcrum's Pociredir Shows Strong Hemoglobin Gains in Sickle Cell Phase 1b Trial

Fulcrum's pociredir shows strong fetal hemoglobin gains in sickle cell Phase 1b trial, with 58% of patients reaching therapeutic levels and reduced pain crises.
FULCrare diseaseclinical trial results