WHO ICTRP trial

A study to evaluate CM24 in combination with nivolumab in adults with solid…

EUCTR2020-005016-21-ES · EU Clinical Trials Register · Authorised

Key facts

Trial ID EUCTR2020-005016-21-ES
Public title A study to evaluate CM24 in combination with nivolumab in adults with solid tumours
Scientific title A Phase 1/2 Study to Assess the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Efficacy of CM24 in combination with nivolumab in adults with advanced solid tumours
Primary sponsor Famewave Ltd.
Registry EU Clinical Trials Register
Recruitment status Authorised
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): yes Therapeutic exploratory (Phase II): yes Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): no
Countries United States;Spain;Israel
Conditions Part A- Recurrent and metastatic non-small cell lung cancer (NSCLC), pancreatic cancer, ovarian cancer, papillary thyroid cancer, colorectal adenocarcinoma and melanoma Part B- Recurrent or metastatic immune checkpoint refractory NSCLC Part…
Interventions Product Code: CM24 Pharmaceutical Form: Solution for infusion INN or Proposed INN: CM24 Other descriptive name: Humanised IgG4k monoclonal antibody against Carcinoembryonic antigen-related cell adhesion molecule 1 Concentration unit: mg/ml…
Registration date Jul 30, 2021
Target size 74
Secondary IDs FW-2020-1
Registry page clinicaltrialsregister.eu

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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