ANS03 for Advanced Solid Tumors with ROS1 or NTRK Alteration

A Study to Investigate ANS03 in Participants With Locally Advanced or Metastatic Solid Tumors

Recruiting Phase 1 Interventional Study
Locally Advanced or Metastatic Solid Tumors Harboring a ROS1 or NTRK Alteration
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
96 (estimated)
Sponsor
Avistone Biotechnology Co., Ltd. · Industry
Who this trial is looking for

This trial is looking for adults with advanced solid tumors that have specific genetic changes (ROS1 or NTRK). Participants will take a medication called ANS03 to see how safe it is and how well it works.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am at least 18 years old
  • I have a life expectancy of at least 12 weeks
  • I have measurable disease according to certain guidelines
  • I have a documented ROS1 or NTRK alteration
  • I have a performance status of 0-2

You may not be able to join if

  • I have an active infection like tuberculosis or HIV
  • I have untreated brain metastases
  • I have serious heart or brain blood vessel diseases
  • I have cancer in the meninges or spinal cord compression

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 a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial

This is a first-in-human Phase I, multi-center, open-label study of ANS03 in patients with advanced solid tumors. The study evaluates the safety, tolerability, preliminary efficay, pharmacokinetics, anti-tumor activity of ANS03 as monotherapy.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Age ≥ 18 years * Eastern Cooperative Oncology Group (ECOG) Performance Status: 0-2 * Life expectancy ≥ 12 weeks * Measurable disease per RECIST v1.1 * Adequate organ and marrow function as defined in the protocol * With documentation of ROS1 or NTRK alteration Exclusion Crite…
Contacts

Avistone Clinical Study Information Center

8610 84148921

information.center@avistonebio.com

CONTACT