Table of Contents
- Trial overview
- Malignant solid tumors study
- Melanoma study
- Non-small cell lung cancer studies
- Main endpoints and what they mean
- Who may take part
Trial overview
The clinical trials in this group study Acasunlimab in people with different types of cancer.[1][2][3][4]
The studies are interventional, which means the researchers give a treatment and then measure the results.[1][2][3][4]
The trial phases range from Phase 1/2 to Phase 3, so the program includes early safety testing and later testing of how well the treatment works.[1][3]
Malignant solid tumors study
NCT03917381 is a Phase 1/2 safety trial in patients with malignant solid tumors.[1]
The cancers listed for this study are endometrial carcinoma, urothelial carcinoma, triple-negative breast cancer, squamous cell carcinoma of the head and neck, and cervical cancer.[1]
The study includes dose escalation, which means the treatment amount is gradually adjusted to find the highest dose that can be given safely.[1]
The brief summary says the study aims to find the maximum tolerated dose, the recommended Phase 2 dose, the safety profile, and clinical efficacy.[1]
The main outcomes include dose-limiting toxicities, adverse events, changes in safety laboratory tests, and objective response rate in an expansion cohort.[1]
Melanoma study
NCT06984328 is a Phase 2 study in advanced cutaneous melanoma, also called skin melanoma.[2]
It includes relapsed/refractory disease, locally advanced unresectable disease, and metastatic disease, which means the cancer came back, did not respond, cannot be removed with surgery, or has spread.[2]
This study tests Acasunlimab alone and together with pembrolizumab.[2]
The main endpoint is objective response rate, measured by the investigator using RECIST v1.1, a standard way to measure tumor changes.[2]
The brief summary says the goal is to evaluate antitumor activity, which means how well the treatment fights the cancer.[2]
Non-small cell lung cancer studies
NCT06635824 is a Phase 3 trial in non-small cell lung cancer.[3]
This study compares Acasunlimab plus pembrolizumab against docetaxel as second- or third-line treatment after prior PD-1/PD-L1 inhibitor therapy and platinum-based standard care.[3]
The main endpoint is overall survival, which looks at how long patients live after treatment starts.[3]
NCT05117242 is a Phase 2 study in relapsed or refractory metastatic non-small cell lung cancer.[4]
It studies Acasunlimab as a single agent or with pembrolizumab, and the main endpoint is objective response rate by investigator review using RECIST v1.1.[4]
Main endpoints and what they mean
The trials use several important endpoints, or main results they want to measure.[1][2][3][4]
Safety endpoints include dose-limiting toxicities, adverse events, and changes in laboratory tests.[1]
Objective response rate shows how many patients had a tumor response, such as complete response or partial response.[1][2][4]
Overall survival is used in the Phase 3 lung cancer study to see whether one treatment helps people live longer.[3]
Who may take part
These trials focus on people with advanced cancer, cancer that has returned, cancer that did not respond to earlier treatment, or cancer that has spread.[2][3][4]
The exact eligibility rules are not fully listed in the source data, so participation depends on the specific trial and cancer type.[1][2][3][4]
The studies also show that Acasunlimab is being tested both by itself and in combination with pembrolizumab, depending on the trial.[2][4]



