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Tag: Solid Tumors

Sigvotatug Vedotin in Previously Treated Metastatic Non-Squamous Non-Small Cell Lung Cancer:...

Sigvotatug Vedotin in Previously Treated Metastatic Non-Squamous Non-Small Cell Lung Cancer: Topline Results from the Phase 3 SigVie-002 Study

AbbVie and RemeGen to Jointly Develop a Novel Bispecific Antibody for...

AbbVie and RemeGen to Jointly Develop a Novel Bispecific Antibody for Advanced Solid Tumors

Pfizer Discontinues Development of Felmetatug Vedotin

In a statement Pfizer confirmed that it has discontinued the development of felmetatug vedotin (also known as PF-08046048 or SGN-B7H4V; see Drugmap).

Tubulis Announces First Patient Dosed in Phase 1/2a Trial Evaluating ADC...

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.

First Patient Dosed in First-in-human trial of AGX101, a Novel ADC...

A first patient has been dosed in a Phase 1 clinical study (NCT06440005) with AGX101, a novel TM4SF1-directed Nuclear-Delivered Antibody-Drug Conjugate™ (ND-ADC) therapy for the treatment of solid tumors. AGX101, which is being developed by privately held biotech startup Angiex, is based on a new, groundbreaking ADC technology platform with a unique mechanisms of action.

FDA Grants Fast Track Designation to Rinatabart Sesutecan for Patients with...

The U.S. Food and Drug Administration (FDA) has granted Fast Track designation for rinatabart sesutecan (Rina-S; PRO1184), a folate receptor alpha (FRα / FOLR1)...

FDA Grants Fast Track Designation to DB-1303 for the Treatment of...

The U.S. Food and Drug Administration (FDA) has granted Fast Track Designation to DB-1303 a novel antibody-drug conjugates for the treatment of patients with advanced, recurrent or metastatic endometrial carcinoma with HER2 over-expression who have progressed on or after standard systemic treatment.

Initial Dose-Escalation of First-in-Human Phase 1 JEWEL-101 Trial Evaluating XB002 in...

An ongoing, phase 1 dose-escalation study investigating XB002, Exelixis’ next-generation tissue factor-targeting antibody-drug conjugate (ADC) for the treatment of patients with advanced solid tumors, has shown promising results.
Featured Image: ADC Therapeutics Booth at AACR 2018 Courtesy: © 2017 – 2018. Sunvalley Communication, LLC / Evan Wendt. Used with permission.

First Patient Dosed in Phase 1 Clinical Trial of ADC Therapeutics’...

A first patient has been dosed in a Phase 1 clinical trial evaluating ADCT-901, targeting kidney-associated antigen 1 (KAAG1), in patients with selected advanced...
Featured Image: Women and the power to fight breast cancer Courtesy: © 2017. Fotolia. Used with permission.

FDA Approves Sacituzumab Govitecan for Adult Patients with Unresectable Locally Advanced...

This week the U.S. Food and Drug Administration (FDA) has granted full approval to Sacituzumab Govitecan* (Trodelvy®; Gilead Sciences) for the treatment of adult...