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BioWorld - Monday, June 29, 2026
Breaking News: FDA says yes to Viridian’s Lumvoa in TEDBreaking News: Science fiction realized: BCI tech is here
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BioWorld, Clinical
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Brain and encephalography

No potassium-bid deficiency as developers channel efforts in Kv7

Jan. 5, 2023
By Randy Osborne
Recent news from Quralis Corp. and Xenon Pharmaceuticals Inc. highlighted the potential for targeting the Kv7 potassium channel, of special interest to a handful of developers lately.
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Geron’s imetelstat IMerges a winner with positive phase III MDS trial

Jan. 4, 2023
By Jennifer Boggs
Geron Corp. executives highlighted a potential billion-dollar market opportunity for imetelstat on the back of positive phase III data for the telomerase inhibitor in patients with lower-risk myelodysplastic syndromes (MDS), news that sent shares (NASDAQ:GERN) rising 36% and could portend the first regulatory win for a scientific approach the company has pursued since the 1990s.
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3D illustration of kidney cross section

Plot thickens as Vera tells phase IIb Origin story with atacicept in IgAN, stays motivated for phase III

Jan. 4, 2023
By Randy Osborne
After Vera Therapeutics Inc.’s disappointing 24-week data from the Origin phase IIb study with atacicept in immunoglobulin A nephropathy (IgAN), Wall Street is looking forward to more results at 36 weeks, due later this year.
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‘Striking outcome’ as Newron reports 6-month data from schizophrenia trial

Jan. 3, 2023
By Nuala Moran
Newron Pharmaceuticals SpA has reported positive six-month data for its selective sodium channel blocker, evenamide, as an add-on therapy to antipsychotic drugs in chronic, treatment-resistant schizophrenia. Patients who had responded at the initial six-week evaluation showed continued improvements in symptoms of psychosis, while others who had not responded at six weeks did so by six months.
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Atrial fibrillation illustration

New research claims cardiac death inconsistencies in Amgen’s phase III Repatha study

Jan. 3, 2023
By Lee Landenberger
New research published in BMJ Open claims there are inconsistencies in Amgen Inc.’s phase III Fourier study for cholesterol lowering. Cardiac deaths were numerically higher in those taking the PCSK9 inhibitor Repatha (evolocumab) combined with a statin than those in the placebo group, the research noted.
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Fresh winds blow in SCD as Jasper airs conditioning-agent data from investigator’s phase I/II bid with briquilimab

Jan. 3, 2023
By Randy Osborne
Jasper Therapeutics Inc. may have found a way around toxicity with current approaches in sickle cell disease (SCD) conditioning approaches, if phase I/II data with briquilimab stay consistent – and the drug already has proved itself across a range of indications. Wall Street liked the prospect, sending the Redwood City, Calif.-based firm’s shares (NASDAQ:JSPR) on a wild ride to close at $2.74, up $2.26, or 476%.
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Hematologic DNA blood test

FIXer upper: Pfizer’s phase III in hemophilia B hits primary endpoint

Dec. 29, 2022
By Lee Landenberger
Little more than a month after the U.S. FDA approved the first gene therapy for adults with hemophilia B, Uniqure NV’s Hemgenix, strong phase III data have come from Pfizer Inc. The Pfizer results show fidanacogene elaparvovec, a vector containing an AAV capsid and a high-activity human coagulation factor IX (FIX) gene for treating adult men with moderately severe to severe hemophilia B, hit the primary endpoint in the phase III Benegene-2 study. The one-time therapy is designed to allow those living with hemophilia B to be able to produce FIX instead of receiving regular, ongoing doses of exogenous FIX.
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Recbio’s COVID-19 vaccine shows strong efficacy in phase II Philippines trial

Dec. 28, 2022
By Doris Yu
Jiangsu Recbio Technology Co. Ltd. released phase II data showing its recombinant two-component COVID-19 vaccine Recov appeared more effective than Comirnaty (tozinameran), the mRNA vaccine developed by Biontech SE and Pfizer Inc., as a booster for users of inactivated vaccines.
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Cytomegalovirus in a human cell

Takeda’s maribavir bested by valganciclovir in post-transplant CMV study

Dec. 22, 2022
By Tamra Sami
Takeda Pharmaceutical Co. Ltd.'s oral antiviral, maribavir, failed to meet the primary endpoint of noninferiority compared to Roche Holding AG’s valganciclovir in the phase III Aurora study for cytomegalovirus (CMV) infection in hematopoietic stem cell transplant recipients. The multicenter, randomized, double-blind, double-dummy, active-controlled study was to form the basis for a future label expansion for the therapy.
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Lung cancer illustration

Tempest TIGIT: New Arcus-Gilead data attempt to steady the space

Dec. 21, 2022
By Lee Landenberger
While new data from Arcus Biosciences Inc. and Gilead Sciences Inc. didn't do much to calm an unsteady development corridor, researcher, developers and analysts still hold out hope for the TIGIT pathway. The Arcus-Gilead randomized phase II study combining anti-TIGIT domvanalimab and anti-PD1 antibodies for treating first-line, metastatic non-small-cell lung cancer produced positive results, including improvements in median progression-free survival (PFS) and six-month landmark PFS rates vs. monotherapy. But a hefty dent in Arcus' shares provide a reminder of TIGIT’s fragility as a field, and a reminder of the phase III failure in May for Roche Holding AG unit Genentech Inc.'s anti-TIGIT immunotherapy tiragolumab, which dragged down the share value of several other class entrants. Arcus stock (NASDAQ:RCUS) dipped deeply on Dec. 20 on the new data’s release, but rallied on Dec. 21 by closing 7.5% upward at $22.15 each.
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