A Study of SGN-CEACAM5C in Adults With Advanced Solid Tumors

NCT06131840 · Status: RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 914

Last updated 2026-04-20

No results posted yet for this study

Summary

This clinical trial is studying advanced solid tumors. Solid tumors are cancers that start in a part of your body like your lungs or liver instead of your blood. Once tumors have grown bigger in one place but haven't spread, they're called locally advanced. If your cancer has spread to other parts of your body, it's called metastatic. When a cancer has gotten so big it can't easily be removed or has spread to other parts of the body, it is called unresectable. These types of cancer are harder to treat.

Participants in this study must have cancer that has come back or did not get better with treatment. Participants must have a solid tumor cancer that can't be treated with standard of care drugs.

This clinical trial uses an experimental drug called PF-08046050. PF-08046050 is a type of antibody-drug conjugate or ADC. ADCs are designed to stick to cancer cells and kill them. They may also stick to some normal cells.

This study will test the safety of PF-08046050 in participants with solid tumors that are hard to treat or have spread throughout the body.

This study has 5 different study parts. Part A and Part B of the study will find out how much PF-08046050 should be given to participants. Part C will use the information from Parts A and B to see if PF-08046050 is safe and if it works to treat certain solid tumor cancers. Part D and E of the study, together with information from Parts A and B, will find out how much PF-08046050 should be given in combination with other anti-cancer agents. Part E will use the information from Parts A, B, and D to see if PF-08046050 is safe in combination with other anti-cancer agents and if it works to treat a certain solid tumor.

Conditions

  • Colorectal Neoplasms
  • Carcinoma, Non-Small-Cell Lung
  • Stomach Neoplasms
  • Pancreatic Ductal Adenocarcinoma
  • Gastroesophageal Junction Adenocarcinoma
  • Small Cell Lung Carcinoma

Interventions

DRUG

PF-08046050

Given into the vein (IV; intravenous)

DRUG

bevacizumab

Given into the vein (IV; intravenous)

DRUG

5-Fluorouracil (5-FU)

Given into the vein (IV; intravenous)

DRUG

Oxaliplatin

Given into the vein (IV; intravenous)

DRUG

Leucovorin (LV)

Given into the vein (IV; intravenous)

Sponsors & Collaborators

  • Sanofi

    collaborator INDUSTRY
  • Seagen, a wholly owned subsidiary of Pfizer

    lead INDUSTRY

Principal Investigators

  • Pfizer CT.gov Call Center · Pfizer

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SEQUENTIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-11-20
Primary Completion
2029-09-12
Completion
2030-09-12
FDA Drug
Yes

Countries

  • United States
  • Canada
  • China
  • France
  • Netherlands
  • Spain
  • Sweden
  • United Kingdom

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06131840 on ClinicalTrials.gov