Clinical Trial Application Submitted for CS5001 (ROR1 ADC) in Combination with First-Line Standard-of-Care for...

Shanghai (China) base CStone Pharmaceuticals has submitted a Phase 1b clinical trial application in Australia for CS5001, a receptor tyrosine kinase-like orphan receptor 1 (ROR1-) targeting antibody-drug conjugate (ADC), in combination with first-line standard-of-care (SoC) for the treatment of Diffuse large B cell lymphoma (DLBCL) is a type of non-Hodgkin lymphoma (NHL).

First Patient Dosed in the WIN-B Trial Exploring the Combination of Debio 0123 +...

A first patients has been dosed in the WIN-B study (NCT06612203)*, a Phase 1b/2, multi-center investigator-initiated trial evaluating the safety and preliminary efficacy of...

Tubulis Announces First Patient Dosed in Phase 1/2a Trial Evaluating ADC TUB-030 in Advanced...

German-based Tubulis continues the expansion of its clinical pipeline with a second ADC drug candidate entering the clinic. Earlier this week the company announced the dosing of the first patient in the 5-STAR-1-01 clinical trial evaluating ADC candidate TUB-030 in solid tumors.
Speakers and attendees during Global Capacity Building Showcase at the American Society of Hematology 61th Annual Meeting at the Orange County Convention Center on Sunday December 8, 2019. Photo Courtesy 2019 © ASH/Nick Agro

Loncastuximab Tesirine Shows Encouraging Results for the Treatment High-risk Follicular Lymphoma and Marginal Zone...

wo clinical trials testing the antibody loncastuximab tesirine (Zynlonta® ADC Therapeutics) showed encouraging results in the treatment of patients diagnosed with high-risk forms of two blood cancers – follicular lymphoma (FL) and marginal zone lymphoma (MZL).

AstraZeneca and Daiichi Sankyo Submit New BLA for Accelerated Approval of Datopotamab Deruxtecan in...

AstraZeneca and Daiichi Sankyo Submit New BLA for Accelerated Approval of Datopotamab Deruxtecan in advanced EGFR-mutated NSCLC

AbbVie Submits BLA to the US FDA for Telisotuzumab Vedotin in Previously Treated NSCLC

AbbVie has submitted a Biologics License Application (BLA) to the U.S. Food and Drug Administration (FDA) for accelerated approval of telisotuzumab vedotin (Teliso-V/ABBV-399; See Drugmap) in adult patients with previously treated, locally advanced or metastatic epidermal growth factor receptor (EGFR) wild type, nonsquamous non-small cell lung cancer (NSCLC) with c-Met protein overexpression.
Astellas Pharma. Exhibition booth during the 2019 annual meeting of the American Society of Medical Oncology (ASCO).

ESMO 2024: Scientific Progress in Advanced and Hard-to-Treat Cancer

During the upcoming annual meeting of the European Society for Medical Oncology (ESMO), being held in Barcelona, September 13-17, 2024, expect presentations to include new data on advances in the treatment of hard-to-treat cancers using approved and investigational agents, including enfortumab vedotin (Padcev™; Astellas/Pfizer/Seagen), Zolbetuximab (previously known as IMAB362), Enzalutamide (Xtandi®; Astellas/Pfizer) and various pipeline products.
Photo: AbbVie R&D has focused on developing biologics. In particular, antibody therapeutics have been proven to be clinically effective for disease areas such as oncology and immunology. Photo courtesy: © 2019 - 2020 AbbVie

ESMO 2024: Showcasing Advancement in ADC Development Pipline with New Data in Tumor...

During the upcoming European Society for Medical Oncology (ESMO) Congress being held in Barcelona, September 13-17, 2024, expect presentations to include new data on...
Featured Image: Women and the power to fight breast cancer Courtesy: © 2017. Fotolia. Used with permission.

Clinical Study finds ADCs to be Highly Effective in Preventing Recurrence in Patients with...

Clinical Study finds ADCs to be Highly Effective in Preventing Recurrence in Patients with Early Stage HER2+ Breast Cancer

Paving the Way: Mirvetuximab Soravtansine + Pembrolizumab in Endometrial Cancer

At the recently held annual meeting of the American Association for Cancer Research (AACR), positive Phase 2 trial (NCT03835819) results of the combination of mirvetuximab soravtansine and the immune checkpoint inhibitor (ICI) Pembrolizumab (Keytruda®; Merck & Co) in the treatment of folate receptor-alpha (FR-α) positive recurrent microsatellite stable / mismatch repair proficient serous endometrial cancer were presented.