A Study With BPI-1178 and Osimertinib in Advanced Non-small Cell Lung Cancer Patients With EGFR Mutations

NCT06362980 | Recruiting Phase 1

• 1 other identifier: BPI-1178-IIT01
• Study Type: interventional
• Target: 20
• Locations: 1 country
• Sites: 1

Brief Summary

BPI-1178 is a novel, orally administered inhibitor of both cyclin-dependent kinase 4 (CDK4) and CDK6 kinase activity. This open-label investigator-initiated trial (IIT) phase I study was designed to evaluate the safety and efficacy of oral BPI-1178 in combination with osimertinib in patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) and epidermal growth factor receptor (EGFR) Mutations.

Conditions

NSCLC

Keywords

NSCLC; EGFR Gene Mutation; BPI-1178; Osimertinib

Outcome Measures

Primary Outcomes (1)

• Number of patients with dose-limiting toxicity (DLT)

  DLT will be evaluated according to the National Cancer Institute Common Terminology Criteria for Adverse Events version 5.0 (NCI CTCAE v5.0).

  From first dosing (Day 7) to Day 28 of Cycle 1 (28 days/cycle)

Secondary Outcomes (10)

• Objective Response Rate (ORR)

  Up to approximately 15 months

• Disease Control Rate (DCR)

  Up to approximately 15 months

• Duration of Response (DoR)

  Up to approximately 15 months

• Progression-Free Survival (PFS)

  Up to approximately 15 months

• Overall Survival (OS)

  Up to approximately 15 months

Study Arms (1)

BPI-1178 plus Osimertinib treatment

EXPERIMENTAL

Patients will undergo treatment with a combination of BPI-1178 capsules and osimertinib tablets. Patients will orally receive a single dose of BPI-1178 (200 or 300 mg) capsules and osimertinib tablets (80 mg). After a 7-day washout period, continuous dosing will commence on the 8th day. During the continuous dosing phase, BPI-1178 capsules and osimertinib tablets will be administered once daily, with a treatment cycle consisting of 28 days.

Drug: BPI-1178; Drug: Osimertinib

Interventions

BPI-1178 DRUG

200 or 300 mg, oral, QD

Also known as: BPI-1178 capsule

BPI-1178 plus Osimertinib treatment

Osimertinib DRUG

80mg, oral, QD

Also known as: Tagrisso

BPI-1178 plus Osimertinib treatment

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Signed written informed consent and ability to comply with the scheduled visits and study procedures outlined in the protocol.
• Age ≥ 18 years, any gender.
• Histologically or cytologically confirmed locally advanced or metastatic non-small cell lung cancer (mainly adenocarcinoma) not suitable for curative surgery or radiation therapy.
• ECOG Performance Status (ECOG PS) score of 0-1. Expected survival of at least 12 weeks.
• Prior treatment with a third-generation EGFR tyrosine kinase inhibitor (TKI) targeted therapy, with radiological evidence of disease progression. The last treatment before enrollment must show radiological evidence of disease progression, intolerance to chemotherapy toxicity, or the patient being ineligible for standard treatment or unable to tolerate the current treatment regimen.
• At least one measurable lesion according to the Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria that has not been previously irradiated.
• Tissue, plasma, or cytological samples collected after disease progression confirmed by imaging following treatment with a third-generation EGFR TKI, demonstrating an EGFR-positive gene mutation sensitive to EGFR TKI treatment (including exon 19 deletion, 21 L858R mutation, etc.), with or without T790M mutation.
• Adequate organ and bone marrow function, with clinical laboratory test results meeting the following criteria:
• Hematology: Neutrophils ≥ 1.5 × 10\^9/L; Platelets ≥ 100 × 10\^9/L; Hemoglobin (Hgb) ≥ 100 g/L;
• Liver function: Total bilirubin (TBIL) ≤ 1.5 × upper limit of normal (ULN) (≤3 × ULN for patients with Gilbert's syndrome); Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 3 × ULN;
• Renal function: Serum creatinine (Cr) ≤ 1.5 × ULN or creatinine clearance rate (CCr, Cockcroft-Gault formula) ≥ 50 mL/min; Semi-quantitative urine testing (e.g., urine dipstick) result showing urine protein \< 2+; patients with urine protein ≥ 2+ at baseline should undergo a 24-hour urine collection, and the protein content in the urine within 24 hours should be \< 1g;
• Coagulation function: Activated partial thromboplastin time (APTT) and international normalized ratio (INR) both ≤ 1.5 × ULN;
• Cardiac function: Left ventricular ejection fraction (LVEF) ≥ 50%;
• At rest, male QTcF \< 450 msec or female QTcF \< 470 msec.
• Ability to swallow oral medications.

You may not qualify if:

• Subjects with any of the following cannot be included in this study:
• History of prior or current use of anti-tumor drugs targeting CDK4/6.
• Individuals with allergies or a history of severe allergic reactions.
• Tissue, plasma, or cytological samples collected after radiological confirmation of disease progression, with testing confirming the presence of specific therapeutic targets such as anaplastic lymphoma kinase (ALK), BRAF V600E, or retinoblastoma (Rb) protein loss.
• Received the last dose of anti-tumor treatment (chemotherapy, targeted therapy, investigational drugs, immunotherapy, tumor embolization, herbal medicine for anti-tumor purposes, etc.) within the 2 weeks preceding the start of study drug administration.
• Presence of third-space effusion (such as significant pleural or abdominal fluid) that cannot be controlled by drainage or other methods.
• Long-term use of steroids is required.
• Unresolved hypokalemia and hypomagnesemia at the time of enrollment.
• Meets any of the following criteria: Various clinically significant arrhythmias and conduction abnormalities, such as atrial fibrillation, complete left bundle branch block, third-degree heart block, second-degree heart block, PR interval \> 250 msec; various factors that may increase the risk of QT interval prolongation or arrhythmia events, such as symptomatic heart failure - New York Heart Association (NYHA) class II-IV, congenital long QT syndrome, Brugada syndrome, history of QT interval prolongation (male \> 470 ms, female \> 480 ms) or torsades de pointes (TdP), family history of long QT syndrome or unexplained sudden death before the age of 40, various concomitant medications that may prolong QT interval; within the 6 months before starting the study drug, had the following diseases, including unstable angina, myocardial infarction, cerebrovascular accident, pulmonary embolism, etc., or underwent cardiac revascularization surgery.
• History of interstitial lung disease, drug-induced interstitial lung disease, radiation pneumonitis requiring steroid treatment, or any clinically evident active interstitial lung disease.
• Known active infections, such as hepatitis B (HBsAg positive and hepatitis B virus (HBV) DNA copy number ≥ 200 IU/ml), hepatitis C, and human immunodeficiency virus (HIV) infection.
• History of allogeneic organ transplantation and allogeneic hematopoietic stem cell transplantation.
• Various factors judged by the investigator to potentially affect the intake and absorption of BPI-1178 or osimertinib, including gastrointestinal factors (such as uncontrolled inflammatory gastrointestinal diseases, history of abdominal fistula or gastrointestinal perforation within 6 months, extensive small intestine resection requiring enteral or parenteral supplementation, inability to swallow, chronic diarrhea, intestinal obstruction, etc.).
• Spinal cord compression, leptomeningeal metastases, or symptomatic brain metastases cannot be included. Asymptomatic patients with brain metastases may be allowed to participate under the following conditions: Asymptomatic brain metastases discovered during screening, determined by the investigator not to require steroids and/or local treatment; asymptomatic brain metastases treated with local therapy (such as radiation) with the patient discontinuing steroids and/or antiepileptic treatment for at least 7 days before the first administration of BPI-1178 in combination with osimertinib.
• Major surgery (craniotomy, thoracotomy, or laparotomy) or severe unhealed wounds, ulcers, or fractures within the 4 weeks preceding the start of study drug administration.

Sponsors & Collaborators

• National Cancer Center, China: lead

Study Sites (1)

National Cancer Center

Beijing, China

RECRUITING

MeSH Terms

Interventions

osimertinib

Study Officials

• Puyuan Xing, Doctorate

  Department of Medical Oncology, National Cancer Center, China

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Puyuan Xing, Doctorate

CONTACT

+86-10-87787421; xingpuyuan@cicams.ac.cn

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Chief Medical Officer

Study Record Dates

• First Submitted: March 28, 2024
• First Posted: April 12, 2024
• Study Start: May 22, 2024
• Primary Completion: April 1, 2025
• Study Completion: April 1, 2026
• Last Updated: July 10, 2024

Record last verified: 2024-07

Data Sharing

• IPD Sharing: Will not share

Locations

CN (1)