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A Study to Evaluate the Safety, Tolerability, Pharmacokinetics (PK), and Antitumor Activity of ALK201 in Participants With Advanced Solid Tumors

trialsTrialRecruiting

A Study to Evaluate the Safety, Tolerability, Pharmacokinetics (PK), and Antitumor Activity of ALK201 in Participants With Advanced Solid Tumors

A phase 1/2 trial of ALK201 in advanced solid tumours, run by Shanghai Allink Biotherapeutics Co., Ltd., now recruiting.

Overview Connected1

Overview

A Study to Evaluate the Safety, Tolerability, Pharmacokinetics (PK), and Antitumor Activity of ALK201 in Participants With Advanced Solid Tumors is a phase 1/2 interventional study registered as NCT06656390 by Shanghai Allink Biotherapeutics Co., Ltd., with 202 participants planned, started 2024-10-24 and due to reach its primary completion in 2027-10-22. Interventions recorded: ALK201.

Setting

A First-in-Human, Open-Label, Multi-Center Phase I/II Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antitumor Activity of ALK201 for Injection in Adult Participants With Advanced Solid Tumors

Phase

Phase 1/2

Sponsor

Shanghai Allink Biotherapeutics Co., Ltd.

Registry

Started

2024-10-24

Enrolled

202 enrolled

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cancers

Metastatic cancer (cancer that has spread)

Evidence strength20/100 · Preliminary

How much and what kind of evidence, not how big the benefit. Click for the breakdown.

Phase 1/2+8
202 enrolled+12
No structured primary endpoint0
Result: recruiting0
No independent replication recorded0

Formula disclosed on the evidence page.

ProvenanceLast edited 2026-09-16 · Jude Gomila · Registry trials wave 6 and products wave 7 · diff · file

Sources & links

ClinicalTrials.gov NCT06656390

Data

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