A Study of YL242 in Subjects With Advanced Solid Tumors

Recruiting Phase 1 Phase 2 Interventional Study
Advanced Solid Tumor
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 1/2
Study type
Interventional
Purpose
Treatment
Participants needed
424 (estimated)
Sponsor
MediLink Therapeutics (Suzhou) Co., Ltd. · Industry
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About This Trial

This is a multicenter, open-label study to evaluate the safety and tolerability of YL242 monotherapy and combination in participants with advanced solid malignant tumors.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Aged ≥18 years. * Eastern Cooperative Oncology Group performance status (ECOG PS) of 0 or 1 * Adequate organ and bone marrow function * Tumor type: Part 1-3: Advanced/unresectable or metastatic solid malignant tumor; Have received at least one prior line of systemic anti-tumo…
Contacts

Medilink Study Team

+86 0512-62858368

clinicaltrials@medilinkthera.com

CONTACT