ANS02 for Non-Small Cell Lung Cancer

Not yet recruiting at 3 trial locations
AC
Overseen ByAvistone Clinical Study Information Center
Age: 18+
Sex: Any
Trial Phase: Phase 1 & 2
Sponsor: Avistone Biotechnology Co., Ltd.
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This is a first-in-human (FIH) Phase I/II, multi-center, open-label, study of ANS02, in patients with advanced NSCLC. The study evaluates the safety, tolerability, preliminary efficay, pharmacokinetics, anti-tumor activity of ANS02 as monotherapy.

Are You a Good Fit for This Trial?

Inclusion Criteria

My life expectancy is at least 12 weeks.
I am fully active or can do light work despite my illness.
* Measurable disease per RECIST v1.1
See 3 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive ANS02 as monotherapy to evaluate safety, tolerability, and preliminary efficacy

Approximately 28 days

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

Long-term Follow-up

Participants are monitored for progression-free survival and overall survival

Approximately 2 years

What Are the Treatments Tested in This Trial?

Interventions

  • ANS02

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: ANS02Experimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Avistone Biotechnology Co., Ltd.

Lead Sponsor

Trials
10
Recruited
1,400+