YL211 for Advanced Solid Tumors

Safety,Tolerability, Pharmacokinetics, and Efficacy of YL211 in Patients With Advanced Solid Tumors

Recruiting Phase 1 Interventional Study
Advanced Solid Tumors
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 1
Study type
Interventional
Purpose
Treatment
Participants needed
500 (estimated)
Sponsor
MediLink Therapeutics (Suzhou) Co., Ltd. · Industry
Who this trial is looking for

This trial is looking for adult patients with advanced solid tumors who have not responded to standard treatments. Participants will take YL211 on its own or in combination with another medication and will need to attend regular check-ups during the study.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am at least 18 years old.
  • I can attend all required visits and procedures.
  • I have advanced solid tumors that did not respond to standard treatments.
  • I have adequate organ and bone marrow function.
  • I have not received certain prior treatments targeting c-MET.

You may not be able to join if

  • I have received continuous systemic steroid therapy for more than 28 days within 28 days prior to the trial.
  • I have a history of leptomeningeal carcinomatosis.
  • I have brain metastasis unless asymptomatic and stable.
  • I have significant ongoing lung disease.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.

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About This Trial
This is a multicenter, open-label, Phase 1 study. The study will enroll subjects with advanced solid tumors. It consists of six parts. Objectives for Dose-Escalation Parts (Part 1 and Part 4) To evaluate the safety and tolerability of YL211 as monotherapy in patients with selected advanced solid tumors (Part 1) and in combination with pembrolizumab in patients with second or third line locally adv…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Informed of the trial before the start of the trial and voluntarily sign their name and date on the ICF. 2. Aged ≥18 years. 3. Be able and willing to comply with protocol visits and procedures. 4. Eastern Cooperative Oncology Group performance status (ECOG PS) of 0 or 5. Adeq…
Contacts

MediLink Study Team

+86 0512-62858368

clinicaltrials@medilinkthera.com

CONTACT