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BioWorld - Tuesday, April 28, 2026
Home » Topics » Clinical

Clinical
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Biotron’s BIT-225 meets endpoints in phase II HIV trial

June 19, 2024
By Tamra Sami
Preliminary data show Biotron Ltd.’s lead compound BIT-225 met the primary objectives of the phase II BIT225-011 trial, a longitudinal, open-label trial designed to characterize the effect of the compound added to ongoing, suppressive antiretroviral therapy in HIV-1-infected, treatment-experienced patients who achieved only partial immune reconstitution.
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Australian coins and bills

Opthea raising AU$227M, enters final phase III stretch for OPT-302

June 18, 2024
By Tamra Sami
Opthea Ltd. announced it plans to raise up to AU$227.3 million (US$150 million) to extend its cash runway through the data readout for its two phase III pivotal trials of sozinibercept (OPT-302) in wet age-related macular degeneration.
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Epileptic brain and abnormal EEG wave discharges

Ovid takes hit on phase III epilepsy failures in Takeda venture

June 18, 2024
By Lee Landenberger
Disappointing top-line data from two failed phase III studies of soticlestat for Dravet syndrome (DS) and Lennox-Gastaut syndrome (LGS) have crumpled the stock of co-developer Ovid Therapeutics Inc., which lost three-quarters of its value June 17.
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Doctor signaling timeout

Two deaths prompt partial clinical holds on three Zentalis studies

June 18, 2024
By Lee Landenberger
The deaths of two cancer patients treated with the small molecule azenosertib has prompted the U.S. FDA to place a partial clinical hold on a phase I study and two phase II studies from Zentalis Pharmaceuticals Inc. The deaths are presumed by Zentalis to be from sepsis. Both patients who died were in the phase II Denali study of platinum-resistant ovarian cancer.
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Madrigal is the NASH/MASH master … of the moment

June 18, 2024
By Lee Landenberger
For the time being, Madrigal Pharmaceuticals Inc.’s Rezdiffra (resmetirom) stands alone as the only U.S. FDA approved treatment for treating nonalcoholic steatohepatitis (NASH). But new and positive data from multiple companies show Madrigal may soon have company.
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Epileptic brain and abnormal EEG wave discharges

Ovid takes hit on phase III epilepsy failures in Takeda venture

June 17, 2024
By Lee Landenberger
Disappointing top-line data from two failed phase III studies of soticlestat for Dravet syndrome (DS) and Lennox-Gastaut syndrome (LGS) have crumpled the stock of co-developer Ovid Therapeutics Inc., which lost three-quarters of its value June 17.
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IBAT they can: Mirum’s volixibat wins in PBC, PSC validate hope

June 17, 2024
By Randy Osborne
Optimism on Wall Street proved wise and shares of Mirum Pharmaceuticals Inc. (NASDAQ:MIRM) rose accordingly to close June 17 at $33, up $7.08, or 27.3%, as the firm disclosed interim results from two phase IIb studies evaluating volixibat, an oral ileal bile acid transporter (IBAT) inhibitor, in patients with primary biliary cholangitis (PBC) and primary sclerosing cholangitis (PSC). The drug proved its mettle in both liver biliary tract-stenosing indications, with no new safety signals turning up, Foster City, Calif.-based Mirum said.
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Arrow missing target

Aerovate plunges on phase IIb miss in pulmonary arterial hypertension

June 17, 2024
By Jennifer Boggs
Aerovate Therapeutics Inc. is shutting down the ongoing phase III portion of its Impahct study of AV-101, an inhaled version of PDGFR inhibitor imatinib, after reporting top-line data from the phase IIb portion failed to meet primary and secondary endpoints in patients with pulmonary arterial hypertension (PAH). It was a major blow for the single-product company, sending shares (NASDAQ:AVTE) falling 93% to close June 17 at $1.65, down $22.97.
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US flag with microscope

US FDA’s Califf hints at more routine use of SGEs at advisories

June 17, 2024
By Mark McCarty
Criticisms over the U.S. FDA’s use of advisory committees led the agency to hold a June 13 public hearing during which FDA commissioner Bob Califf said the agency is working to improve the experience of special government employees who take part in these hearings.
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Man scratching back

Itch takes a powder as Cara scratches difelikefalin

June 13, 2024
By Karen Carey
Following a phase II/III failure, Stamford, Conn.-based Cara Therapeutics Inc. discontinued its only pipeline program, that of oral difelikefalin for moderate to severe pruritis in adults with notalgia paresthetica, placing the company’s future in question.
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