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BioWorld - Sunday, March 1, 2026
Home » Topics » Clinical, BioWorld

Clinical, BioWorld
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Kadmon TCT data provide ‘Incyte,’ GVHD odds looking better

Feb. 27, 2020
By Randy Osborne
New York-based Kadmon Holdings Inc.’s recent oral late-breaker session on KD-025 in chronic graft-vs.-host disease (cGVHD) at the Transplantation & Cellular Therapy (TCT) meeting – along with data that rolled out from two studies testing competitor Jakafi (ruxolitinib) from Incyte Corp. – signaled potential advantages in the former’s candidate, already highly regarded.
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Menlo, Vanda see mixed results after missing primary endpoints in pruritus trials

Feb. 26, 2020
By Michael Fitzhugh
Readouts from two ambitious pruritus trials this week yielded starkly different reactions from investors seeking broader meaning in the outcomes.
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Architectural pillars

Judge orders HHS to fill 10-year data gap on Clinicaltrials.gov

Feb. 26, 2020
By Mari Serebrov
While the staff at the U.S. Department of Health and Human Services (HHS) is currently all hands-on-deck in responding to the COVID-19 outbreak, some of the agencies in the department may have to divert resources to get sponsors of drug and device clinical trials to fill in nearly a decade-long data gap on Clinicaltrials.gov. That’s if a judge’s decision handed down this week stands.
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Immutep reports positive interim phase II results in Keytruda combo basket trial

Feb. 26, 2020
By Tamra Sami
PERTH, Australia – Sydney-based Immutep Ltd. reported positive interim data for its phase II basket trial in non-small-cell lung cancer (NSCLC) and head and neck squamous cell carcinoma for its lead immunotherapy in combination with Merck & Co. Inc.’s anti-PD-1 therapy, Keytruda (pembrolizumab).
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Shock away? Adrenomed’s adrecizumab hits phase II endpoint in septic shock

Feb. 26, 2020
By Cormac Sheridan
DUBLIN – Adrenomed AG disclosed Feb. 21 that its first-in-class antibody, adrecizumab, hit the primary safety and tolerability endpoint of a phase II trial in septic shock.
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IMV’s phase II ovarian cancer data trend positive while the stock reverses

Feb. 25, 2020
By Lee Landenberger
Updated results from IMV Inc.’s ongoing phase II trial of DPX-Survivac to treat advanced recurrent ovarian cancer show the company’s lead candidate was active and well-tolerated in patients.
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NGM studios’ top-line phase II NASH premiere whets appetite for Alpine 2/3 sequel

Feb. 24, 2020
By Randy Osborne
NGM Biopharmaceuticals Inc. wowed investors with positive preliminary top-line results from the 24-week double-blind, randomized, placebo-controlled fourth cohort of an adaptive phase II study testing aldafermin in nonalcoholic steatohepatitis (NASH).
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VMAT2 carry-through brings Waterloo for Austedo TS bid by Teva

Feb. 20, 2020
By Randy Osborne
Teva Pharmaceutical Industries Ltd.’s Austedo (deutetrabenazine) lived up to the lack of expectations in pediatric Tourette syndrome (TS), missing identical primary endpoints in a pair of late-stage trials.
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Zelira’s medicinal cannabis therapy meets primary endpoints in phase I/II insomnia trial

Feb. 20, 2020
By Tamra Sami
PERTH, Australia – Medicinal cannabis company Zelira Therapeutics Ltd. reported that its ZLT-101 therapy met the primary endpoint of a statistically significant improvement in insomnia in a phase Ib/IIa study in patients diagnosed with chronic insomnia.
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Newco news

Reinvented Coimmune has a new IND and two clinical trials

Feb. 19, 2020
By Lee Landenberger
It’s been a rapid year of change for Coimmune Inc., which was incorporated only 12 months ago and now has FDA approval of an IND clearing the way for a phase IIb trial using CMN-001 to treat advanced metastatic renal cell carcinoma (mRCC).
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