U.S., July 11 -- ClinicalTrials.gov registry received information related to the study (NCT07694765) titled 'A Study of LM-364 as a Single Agent or in Combination With Anti-tumor Therapy in Patients With Advanced Solid Tumors' on July 03.
Brief Summary: For Phase I, to assess the safety and tolerability, obtain the recommended phase 2 dose (RP2D)/optimal biologic dose (OBD) and/or Maximum Tolerated Dose (MTD) for LM-364 as a single agent or in combination with tislelizumab in participants with advanced solid tumors.
For Phase II, to assess the preliminary anti-tumor activity of IMP in participants with advanced solid tumors.
Study Start Date: July 15
Study Type: INTERVENTIONAL
Condition:
Malignant Tumors
Intervention:
DRUG: LM-364 f...