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Study details
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Study of Anti-CEACAM5 ADC M9140 in Participants With Advanced Solid Tumors (PROCEADE PanTumor)

EMD Serono Research & Development Institute, Inc.
NCT IDNCT06710132ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1/2

Target enrollment

250

Study length

about 3 years

Ages

18+

Locations

11 sites in CA, DC, FL +4

What this study is about

Researchers are testing a new treatment, M9140, for advanced solid tumors that express CEACAM5. The goal is to see if this treatment works, is safe, and how it affects the body. The trial will include participants with gastric cancer, non-small cell lung cancer (NSCLC), pancreatic cancer, or pancreatic ductal adenocarcinoma (PDAC).

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take M9140

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Substudies GC/NSCLC/PDAC: Objective Response (OR) According to Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1) as Assessed by Investigators

Secondary: Substudies GC/ NSCLC/ PDAC: Pharmacokinetic (PK) Plasma Concentrations of M9140, Substudies GC/NSCLC/PDAC: Duration of Response (DoR) According to Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1) as Assessed by Investigators, Substudies GC/NSCLC/PDAC: Number of Participants with Adverse Events (AEs) and Treatment Related AEs, Substudies GC/NSCLC/PDAC: Progression-free Survival (PFS) According to Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1) as Assessed by Investigators

Body systems

Oncology