A Study of BMS-986490 With or Without Bevacizumab in Advanced Solid Tumors

Trial statusRecruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorBristol-Myers Squibb

About this trial

This is a study of BMS-986490 as a monotherapy and in combination with bevacizumab in participants with select advanced solid tumors known to express CEACAM5.

Eligibility criteria

Qualifiers

Documented histologically or cytologically confirmed, advanced, unresectable/metastatic solid tumor measurable by RECIST v1.1.

Disqualifiers

History of anaphylactic reactions to irinotecan and/or bevacizumab.

Previously received therapy targeting CEACAM5.

Grade ≥3 ILD/pneumonitis.

Other protocol-defined Inclusion/Exclusion criteria apply.

Trial design

Treatments tested in this trial

  • BMS-986490
  • Bevacizumab

Treatment groups

360 Participants
are divided into 5 treatment groups

Locations

6
Australia
Tasman Oncology Research4215, SouthportQueensland, Australia
Canada
Princess Margaret Cancer CentreM5G 2M9, TorontoOntario, Canada
United States
Local Institution - 000790033, Los AngelesCalifornia, United States
Local Institution - 001749546, Grand RapidsMichigan, United States

Sponsors and collaborators

Bristol-Myers Squibb

Lead sponsor