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BioWorld - Saturday, January 10, 2026
Home » Topics » Clinical

Clinical
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Innovent scores first IND for TIGIT antibody and explores PD-1/RNAi combination

Jan. 14, 2020
By Elise Mak
China-based Innovent Biologics Inc. will need to get on two new tasks this year: Preparing for the first clinical trial for an anti-TIGIT antibody in China and investigating the combination therapy of its Tyvyt (sintilimab) and Sirnaomics Inc.’s STP-705.
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Abbott gets FDA OK to start Mitraclip study in moderate surgical risk patients

Jan. 13, 2020
By Liz Hollis
Abbott Park, Ill.-based Abbott Laboratories has gained the U.S. FDA’s nod for a clinical trial that will compare the effectiveness of Mitraclip to open-heart mitral valve surgical repair in people with primary mitral regurgitation (MR) who are eligible for open-heart surgery. The prospective, randomized REPAIR MR clinical trial is expected to enroll 500 patients.
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'Holy grail'

Adaptimmune SPEARs 4 partial responses in various tumor types

Jan. 13, 2020
By Brian Orelli
While companies have seen plenty of success treating blood cancers with T-cell therapies, solid tumors have largely remained the holy grail for T cells. But Adaptimmune Therapeutics plc has early data from its Specific Peptide Enhanced Affinity Receptor T-cell platform suggesting it may be on the right path for a platform with a wide breadth.
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Fish oil capsules

Mine, oil mine? Amarin CV fish rivals sink as generic-makers angle for catches in IP

Jan. 13, 2020
By Randy Osborne
With a label broadened by the FDA in December and two aspiring competitors apparently picked off via late-stage trial blowups, Amarin Corp. plc finds itself in strong position with fish oil therapy Vascepa  (icosapent ethyl) – at least pending the outcome of court proceedings that involve challengers to patents for the cardiovascular (CV) drug.
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Verona climbs on solid phase IIb data for COPD therapy; phase III to start this year

Jan. 13, 2020
By Nuala Moran
LONDON – Verona Pharma plc reported positive phase IIb results for the nebulized formulation of its dual phosphodiesterase (PDE) 3 and 4 inhibitor, ensifentrine (RPL-554), as an add-on to standard bronchodilation therapy in chronic obstructive pulmonary disorder (COPD).
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Kandy’s nonhormonal menopause therapy hits primary and secondary endpoints in phase IIb

Jan. 13, 2020
By Nuala Moran
LONDON – Kandy Therapeutics Ltd. has announced positive results for its nonhormonal treatment for menopause symptoms, showing a reduction in the number of hot flashes and night sweats, and a positive effect on secondary endpoints relating to mood and quality of life.
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Innovent scores first IND for TIGIT antibody and explores PD-1/RNAi combination

Jan. 13, 2020
By Elise Mak
BEIJING – China-based Innovent Biologics Inc. will need to get on two new tasks this year: Preparing for the first clinical trial for an anti-TIGIT antibody in China and investigating the combination therapy of its PD-1 antibody, Tyvyt (sintilimab), and Sirnaomics Inc.’s RNAi drug candidate, STP-705.
Read More
Let them eat steak

Ultragenyx flying high on responders to its gene therapy for ornithine transcarbamylase deficiency

Jan. 10, 2020
By Brian Orelli
The prospects for Ultragenyx Pharmaceutical Inc.'s adeno-associated virus (AAV) gene therapy, DTX-301, in patients with ornithine transcarbamylase (OTC) deficiency weren't looking too great after treatment of the first two cohorts in a phase I/II study.
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Galactose skeletal formula

Agent 007’s efficacy in galactosemia no secret; ATI Bond for meeting with FDA

Jan. 8, 2020
By Randy Osborne
Applied Therapeutics Inc. (ATI) CEO Shoshana Shendelman said positive top-line findings with aldose reductase inhibitor AT-007 in galactosemia were “the data we needed, and we’re going to move as quickly as we can to get in and speak to the FDA about this, not only to firm up our NDA filing but also to get into the pediatric study.”
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Biodegradable polymer stents show well in study against durable polymers

Jan. 7, 2020
By Mark McCarty
While the disappearing drug-eluting stent seems to have faded from view for the time being, several manufacturers have invested in fabrication of drug-eluting stents with polymers that absorb once the drug of elution has done its work. A new study indicates that patients who have already had a myocardial infarction fare better on stents made with these biodegradable polymers, an outcome that may soon push second-generation DES devices into med-tech history.
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