A First-in-Human Dose Escalation and Expansion Study to Evaluate Intratumoral Administration of SAR441000 as Monotherapy and in Combination With Cemiplimab in Patients With Advanced Solid Tumors
Stopped Sponsor terminated the study for non-safety reasons
Conditions
Interventions
- DRUG: SAR441000
- DRUG: Cemiplimab REGN2810
Sponsor
Sanofi
Collaborators