Study of the Safety Pharmacokinetics Pharmacodynamics and Preliminary Clinical Activity of RP-6306 in Patients with Advanced Solid Tumors (MYTHIC Study)
Recruiting
12 years - 99 years
All
Phase
1
10 participants needed
1 Location
Brief description of study
The primary purpose of this study is to assess the safety and tolerability of an Investigational drug in patients with eligible advanced solid tumors, determine the maximum tolerated dose (MTD) and assess preliminary anti-tumor activity.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Advanced Solid Tumor
-
Age: 12 years - 99 years
-
Gender: All
Male or female and ≥12 years-of-age, advanced or metastatic resistant or refractory solid tumors.
Updated on
04 Aug 2024.
Study ID: 849282