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BioWorld - Tuesday, February 3, 2026
Home » Topics » Conferences, BioWorld

Conferences, BioWorld
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Gamma secretase protein complex

ESMO 2022: For gamma secretase inhibitors, a better second act in cancer?

Sep. 12, 2022
By Anette Breindl
The gamma secretase inhibitor nirogacestat (Springworks Therapeutics Inc.) reduced the risk of disease progression by roughly 70% in a randomized placebo-controlled phase III trial in patients with desmoid tumors.
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ESMO 2022: Slicing away at KRAS, one trial at a time

Sep. 12, 2022
By Anette Breindl
Data presented Sept. 9 at the European Society of Medical Oncology 2022 Congress showed impressive effects for KRAS inhibitors. But they also illustrated their limitations. Earlier-stage trials and researcher presentations, meanwhile, suggested ways those limitations might be addressed. Results from the Codebreak 200 study, presented in the day’s Presidential Symposium, were typical of the best that targeted therapies have to offer: large effects for brief time periods.
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Natural killer cell attacking cancer cell

ESMO 2022: First phase III success for cell therapy in solid tumors

Sep. 12, 2022
By Anette Breindl
Scientifically at least, the biggest story coming out of the European Society for Medical Oncology (ESMO) 2022 Congress is the success of cell therapy in solid tumors. “During this ESMO, there is a lot of novelty coming from T-cell therapies,” John Haanen told the audience at his joint keynote speech with Ton Schumacher – so much so that Haanen and Schumacher, both group leaders at the Netherlands Cancer Institute, left antibodies out of their keynote session in order to do justice to the advances in cell therapies.
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ESMO 2022: Catalym’s first-in-class GDF-15 inhibitor shows signs of activity in late-stage cancer patients

Sep. 12, 2022
By Cormac Sheridan
Catalym GmbH reported in an oral session at the European Society for Medical Oncology meeting in Paris that its first-in-class growth differentiation factor 15 inhibitor, visugromab, demonstrated preliminary signs of efficacy in a heavily pretreated group of cancer patients who were resistant or refractory to checkpoint inhibitors.
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Conference data for Sept. 12, 2022: ESMO

Sep. 12, 2022
New and updated preclinical and clinical data presented by biopharma firms at the European Society for Medical Oncology Congress 2022, including: Adaptimmune, Curelab, Novartis.
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Vial and syringe with DNA
European Society for Medical Oncology 2022

Genexine’s therapeutic DNA vaccine could extend survival in late-stage cervical cancer

Sep. 9, 2022
By Tamra Sami
Genexine Co. Ltd.’s DNA vaccine, GX-188E, showed potential in extending overall survival in patients with advanced cervical cancer in a phase II study when given in combination with Merck & Co. Inc.’s anti-PD-1 therapy, Keytruda (pembrolizumab).
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Conference data for Sept. 9, 2022: ESMO

Sep. 9, 2022
New and updated preclinical and clinical data presented by biopharma firms at the European Society for Medical Oncology Congress 2022, including: Debiopharm, Elevar, Genexine, Gilead, Hutchmed, Innovent.
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ESMO 2022

First phase III success for cell therapy in solid tumors

Sep. 8, 2022
By Anette Breindl
ESMO late breakers were released Sept. 8, and scientifically at least, a key theme of the meeting will be that cell therapies, at long last, are capable of besting solid tumors.
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HKEX exterior

HKEX Biotech Summit 2022 zooms in on biopharma investment trends

Sep. 2, 2022
By Doris Yu
Investments in early stage biotech companies were in focus at the Hong Kong Stock Exchange’s (HKEX) Biotech Summit 2022. The virtual event on Sept. 1 saw discussions centered on this investment trend for younger biotech firms, which looks to be where capital is headed in the sector after a cooldown for listings in Chinese stock markets in the first half of 2022.
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European Union flag
Advanced Therapies Europe 2022

Regulators play catch-up as advanced therapy research races forward

Sep. 1, 2022
By Richard Staines
Regulation of advanced therapies has come under scrutiny at a conference in London, as activity in the sector heats up amid Europe’s root and branch review of pharmaceutical legislation.
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