Recruiting
Phase 1

PLB1004

Sponsor:

Avistone Biotechnology Co., Ltd.

Code:

NCT06046495

Conditions

Non-Small Cell Lung Cancer

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

PLB1004

Study Details

Brief summary:

This is a Phase I, multicenter, open-label, dose escalation and dose expansion study to assess the safety and pharmacokinetic profile of PLB1004, a mono-anilino-pyrimidine compound, given alone in NSCLC patients with EGFR exon 20 insertion mutations,uncommon mutations, classical mutations (Ex19del and L858R), and drug-resistant mutation (T790M). Patients will be enrolled and dosed according to the most current protocol. This study is made of two Parts. Part 1 includes a dose escalation into 7 cohorts and patient allocation to these cohorts will be via slot allocation. Each cohort has a minimum of 3 and a maximum of 6 patients for a total of 21 - 42 patients. The patient population of the dose escalation phase will include patients with advanced NSCLC harboring EGFR classical mutations or Ex20ins mutations, or uncommon mutations. Part 2 includes an expansion phase and the expansion phase will explore one or more dose levels of PLB1004 in NSCLC patients with EGFR Ex20ins mutations, classical mutations, or uncommon mutations.

Conditions

Non-Small Cell Lung Cancer

Study ID

NCT06046495

Start date

Jul 8, 2024

Status verified date

Apr, 2025

Completion date

Feb 9, 2028

Anticipated

Primary completion date

Feb 9, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. Ability to understand and willingness to sign a written informed consent document;
2. Male or female adult patients 18 years of age or older;
3. Patients should have recovered from toxicities related to prior anti-tumor therapy;
4. Patients should have recovered from the effects of major surgery;
5. Have a documented EGFR mutation by a local test in tissue or plasma;
6. At least 12 weeks life expectancy;
7. Must have at least one measurable lesion per RECIST v 1.1;
8. Sexually active males and females of childbearing potential must agree to take effective contraceptive measures.

Exclusion Criteria:

1. Received radiotherapy within 14 days before enrollment;
2. Have significant or uncontrolled systemic disease;
3. Have significant or uncontrolled cardiovascular disease;
4. Have had other diagnosed malignant diseases that required treatment within the past 3 years besides NSCLC;
5. Currently have or had a history of interstitial lung disease, drug-induced interstitial lung disease, or radiation pneumonia that requires steroid therapy;
6. Have known hypersensitivity to the similar drugs and excipients of PLB1004;
7. Pregnant or lactating women;
8. Have used other experimental drugs within 2 weeks prior to the first dose of PLB1004;
9. Have any condition or illness that could affect the compliance with the protocol.

Study Design

Enrollment

81 participants

Anticipated

Intervention Model

Sequential

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: PLB1004

PLB1004 given as a mono-therapy in dose escalation and dose expansion phase.

Interventions

PLB1004

PLB1004 will be orally self-administered by the patient as a mono-therapy.

Primary outcome measure

  • Safety profile of PLB1004 per CTCAE v5.0 [ Time Frame: Up to 2 years ]

Central Contacts and Locations

Central contacts

Avistone Clinical Study Information Center Center

+86-10-84148921information.center@avistonebio.com

Locations

University of California-Davis

Recruiting

Sacramento, California, United States, 95817-1514

Research Site

Recruiting

Louisville, Kentucky, United States, 40202

Nebraska Cancer Specialists

Recruiting

Omaha, Nebraska, United States, 68130

Research Site

Recruiting

New York City, New York, United States, 100021

Sarah Cannon Research Institute

Recruiting

Nashville, Tennessee, United States, 37203

Swedish Health Sciences

Recruiting

Seattle, Washington, United States, 98122

Research Site

Recruiting

Seattle, Washington, United States, 98195

More Information

Sponsor

Avistone Biotechnology Co., Ltd.

Last update posted

Apr 23, 2025

Last verified

Apr, 2025

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Avistone Biotechnology Co., Ltd. on 2025-04-23.