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BioWorld - Wednesday, February 25, 2026
Home » Topics » Clinical, BioWorld Asia

Clinical, BioWorld Asia
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Jacobio’s KRAS G12C inhibitor progresses to pivotal trials in China for pancreatic cancer

July 11, 2023
By Tamra Sami
China’s Center for Drug Evaluation has cleared Jacobio Pharmaceuticals Group Co. Ltd.’s KRAS G12C inhibitor, glecirasib (JAB-21822), to begin a phase III pivotal study for pancreatic cancer.
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Antibody
Newco news

Haemalogix’s Kappamab hits endpoints in phase IIb myeloma trial

July 11, 2023
By Tamra Sami
Haemalogix Ltd.’s monoclonal antibody Kappamab met all primary endpoints in a phase IIb trial that combined the MAb with lenalidomide and dexamethasone in kappa-type multiple myeloma patients who had relapsed or become refractory to other treatments.
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Xray showing lung cancer on tablet

Astrazeneca, Daiichi won’t cop to TROP2 grade 5s; OS data from phase III yet to emerge

July 11, 2023
By Randy Osborne
The trophoblast cell surface antigen 2 (TROP2) class chalked mix news by way of Astrazeneca plc and Daiichi Sankyo Co. Ltd. as the pair disclosed phase III data from the closely watched Tropion-Lung 1 trial with datopotamab deruxtecan (dato-dxd) against non-small-cell lung cancer.
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Illustration of intestines with inflammation
Newco news

Microba enters clinic with gut microbiome-derived therapy for inflammatory bowel disease

July 11, 2023
By Tamra Sami
Microba Life Sciences Ltd. has started dosing patients in a phase I trial of its gut microbiome-derived therapeutic, MAP-315, for ulcerative colitis, the major form of inflammatory bowel disease (IBD).
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Transcenta’s osemitamab on track for pivotal gastric cancer trials in Korea, China

July 11, 2023
By Tamra Sami
China’s Center for Drug Evaluation and South Korea’s Ministry of Food and Drug Safety cleared Transcenta Holdings to begin phase III pivotal trials of osemitamab (TST-001) in combination with nivolumab and chemotherapy for first-line treatment of HER2-negative, Claudin 18.2 expressing locally advanced or metastatic gastric or gastroesophageal cancer.
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Moderna hits global stride with transatlantic RSV vaccine regulatory filing, China R&D investment

July 11, 2023
By Marian (YoonJee) Chu
Moderna Inc. may have risen to prominence during the pandemic with its messenger RNA (mRNA)-based COVID-19 vaccine, but it’s now casting a net far larger and wider. The company said on July 5 that it is readying international approval for its second mRNA vaccine called mRNA-1345 for respiratory syncytial virus (RSV)-associated acute respiratory disease based on positive interim data from the ongoing Conquer RSV study in individuals 60 and older.
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Skin irritation on hands

Aslan shares slide on mixed phase IIb data for eblasakimab, chasing Dupixent in atopic dermatitis

July 11, 2023
By Marian (YoonJee) Chu
Aslan Pharmaceuticals Pte. Ltd. announced variegated results from its phase IIb TREK-AD trial testing eblasakimab, its biologic tested for moderate to severe atopic dermatitis (AD), that drew an equally mixed reaction from the market.
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Eucorvac-19

Eubiologics to file for COVID-19 vaccine approval in Philippines with positive interim phase III data

June 27, 2023
By Marian (YoonJee) Chu

Eubiologics Co. Ltd. said it would file for regulatory approval for its COVID-19 vaccine called Eucorvac-19 in the Philippines, after announcing positive interim phase III trial results on June 27.


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Brain activity concept illustration
Newco news

Enveric Biosciences gears up for phase I anxiety trial with psilocin prodrug

June 27, 2023
By Tamra Sami
Enveric Biosciences Inc. is gearing up to begin clinical trials in generalized anxiety disorder with lead candidate, EB-373, a psilocin prodrug. Trials are expected to begin in the fourth quarter of 2023.
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Squamous cell carcinoma.

Sirnaomics advances siRNA skin cancer candidate to late-stage trials

June 20, 2023
By Tamra Sami
Sirnaomics Ltd. is advancing lead siRNA candidate STP-705 for the treatment of squamous cell carcinoma in situ into late-stage clinical testing after sharing encouraging phase II trial results with the U.S. FDA in an end-of-phase II meeting. The company plans to move forward in 2023 with a single-dose study as a subgroup of subjects in a large phase III study. Positive results will provide the basis for completion of this large registrational phase III trial.
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