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Study details
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A Study to Evaluate the Safety, Tolerability, Pharmacokinetics (PK), and Antitumor Activity of ALK202 in Participants with Advanced Solid Tumors

Shanghai Allink Biotherapeutics Co., Ltd.
NCT IDNCT06707610ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

234

Study length

about 3.9 years

Ages

18–75

Locations

2 sites in FL, VA

What this study is about

This trial is testing a treatment called ALK202 for people with advanced solid tumors. The goal is to see if it's safe, well-tolerated, how the body processes it (pharmacokinetics), and whether it fights cancer cells (antitumor activity).

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take ALK202

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Standard

How treatment is administered

Treatment Assignment
Standard assignment

Assignment is predetermined by the study protocol.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: To evaluate the safety and tolerability of ALK202 in adult participants with advanced solid tumors; To determine the maximum tolerated dose (MTD); To determine the recommended dose(s) of ALK202 for subsequent clinical studies.

Secondary: To evaluate the pharmacokinetics (PK) of ALK202

Body systems

Oncology