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BioWorld - Sunday, May 10, 2026
Home » Topics » Cancer, BioWorld Asia

Cancer, BioWorld Asia
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Astellas’ Claudin 18 inhibitor meets primary endpoint in phase III gastric cancer trial

Nov. 22, 2022
By Tamra Sami
Astellas Pharma Inc.’s zolbetuximab, a monoclonal antibody targeting Claudin 18.2, met the primary endpoint of progression-free survival in the phase III Spotlight trial in CLDN18.2-positive, HER2-negative, locally advanced unresectable or metastatic gastric or gastroesophageal junction adenocarcinoma, according to top-line data.
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Xray showing lung cancer on tablet

Immutep’s LAG-3 efti, with pembrolizumab, meets primary endpoint in first-line NSCLC

Nov. 15, 2022
By Tamra Sami
Immutep Ltd.’s lead immunotherapy candidate eftilagimod (IMP-321, efti) met the primary endpoint in its phase II trial evaluating the combination of efti and Merck & Co. Inc.’s Keytruda (pembrolizumab) as first-line treatment of non-small-cell lung cancer (NSCLC), reporting final data that show an overall response rate of 40.4%.
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Health professional recording info from patient

Que sees phase II success in reducing hot flashes after breast cancer

Nov. 15, 2022
By Tamra Sami
Que Oncology Inc.’s Q-122 significantly reduced the frequency and severity of moderate and severe vasomotor symptoms, or hot flashes, in women taking endocrine therapy for breast cancer, and phase II results showed associated improvement in quality of life, compared with placebo.
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Ovarian cancer illustration

GSK’s PARP inhibitor limited in ovarian cancer after FDA OS review

Nov. 15, 2022
By Jennifer Boggs
GSK plc said it will restrict the second-line maintenance indication for ovarian cancer drug Zejula (niraparib) to only patients with deleterious or suspected germline BRCA mutations, at the request of the FDA, in a sign that U.S. regulators aren’t going to relax scrutiny on PARP inhibitors any time soon.
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Kidneys

Telix’s imaging agent meets primary, secondary endpoints in phase III kidney cancer trial

Nov. 8, 2022
By Tamra Sami
Radiopharmaceutical company Telix Pharmaceuticals Ltd’s TLX250-CDx (Zirconium (89Zr) TX250) met both primary and secondary endpoints in the phase III Zircon study in clear cell renal cell carcinoma, according to top-line data.
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Biocytogen out-licenses CD40 antibody to Isu Abxis to develop trispecific antibodies

Nov. 8, 2022
By Doris Yu
Biocytogen Pharmaceuticals Co. Ltd.’s subsidiary Eucure Biopharma Co. Ltd. has granted Isu Abxis Co. Ltd. rights to use its humanized agonistic anti-CD40 antibody YH-003 to develop cancer drugs.
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Glass yen/yuan symbol

Beihai Biotech nets nearly ¥200M to support core asset development

Nov. 8, 2022
By Doris Yu
Zhuhai Beihai Biotech Co. Ltd. has raised nearly ¥200 million (US$27.5 million) in a series B round slated to support clinical trials for its lead candidates as well as preparations to file an NDA for its core asset, BH-009.
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The Combat of Rama and Ravana.
Cancer

ENA 2022: Mutant specific or target selective, that is the question for drug development

Nov. 1, 2022
By Mar de Miguel and Anette Breindl
Diwali, the Festival of Light, marks different events depending on where it is celebrated. In some areas of India, it marks the return of Lord Rama to his birthplace of Ayodhya after defeating the demon Ravana.
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Maxinovel raises ¥100M in series C+ financing

Oct. 25, 2022
By Doris Yu
Maxinovel Pharmaceuticals Inc. raised ¥100 million (US$13.8 million) in a series C+ round to develop its candidates for acute myeloid leukemia, solid tumors, and autoimmune diseases.
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Tasigna.png

First cancer drug licensing agreement a big splash in global patent pool

Oct. 25, 2022
By Mari Serebrov
Expanding its mandate to accelerate access to essential medicines to people in low- and middle-income countries, the Medicines Patent Pool signed its first voluntary licensing agreement for a cancer treatment, Novartis AG’s Tasigna (nilotinib).
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