Safety, Tolerability and Pharmacokinetic Profile of BPI-15086 in EGFR T790M Mutation-positive NSCLC Patients

NCT02914990 | Completed Phase 1 DMC

• 1 other identifier: BTP-26511
• Study Type: interventional
• Target: 36
• Locations: 1 country
• Sites: 1

Brief Summary

The main objective of this study is to evaluate the safety and tolerability of BPI-15086.

Conditions

Non-Small Cell Lung Cancer

Outcome Measures

Primary Outcomes (1)

• Adverse events

  Adverse events were graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events, version 4.03

  18 months

Secondary Outcomes (5)

• Cmax

  4 weeks

• Half life

  4 weeks

• AUC

  4 weeks

• Objective Response Rate

  12 weeks

• Progression-Free Survival

  18 months

Study Arms (1)

BPI-15086

EXPERIMENTAL

BPI-15086, orally administered daily

Drug: BPI-15086

Interventions

BPI-15086 DRUG

BPI-15086 is administered once daily with a starting dose of 25 mg in a 21-day cycle. When tolerated, increasing doses of BPI-15086 will be tested in subsequent cohorts, until a maximum tolerated dose is determined.

BPI-15086

Eligibility Criteria

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

You may qualify if:

• Histologically or cytologically confirmed, locally advanced or metastatic NSCLC patients, who is not suitable for surgery or radiotherapy
• Radiological documentation of disease progression while on a previous continuous EGFR TKI (e.g. icotinib, gefitinib, afatinib, neratinib, dacomitnib, or erlotinib) treatment
• Patients must fulfil one of the following:
• Confirmation that the tumour harbours EGFR sensitivity mutation (exon 19 deletion, L858R and L861R, G719X)
• Must have experienced clinical benefit from EGFR TKIs, according to the Jackman criteria
• Confirmation of T790M mutation positive after disease progression on EGFR TKIs
• Eastern Cooperative Oncology Group (ECOG) performance status of 0-2 and estimated life expectancy of at least 12 weeks
• Measurable lesion per Response Evaluation Criteria in Solid Tumors(RECIST1.1)
• Adequate bone marrow, hepatic, and renal function
• Women: For pre-menopausal women who have a childbearing potential, they must have a pregnancy test within 7 days before starting treatment. The serum or urine pregnancy test must be negative and must be non-lacking; all patients (whether male or female) should be Adequate barrier contraceptive measures during the entire treatment period and 3 months after the end of treatment
• Have signed Informed Consent Form

You may not qualify if:

• Any other malignancy within 5 years of the first dose of study treatment
• Radiotherapy for target lesion within 4 weeks of the first dose of study treatment.
• From the treatment of reversible EGFR TKI drugs (e.g. Ectinib, Gefitinib, Erlotinib) to the first use of drugs, the time did not exceed 8 days or 5 half-lives (take the long time)；Irreversible EGFR TKI drugs (e.g. Alfatinib, Neratinib, Dacomitinib) did not last more than 14 days or 5 half-lives (take the long term)
• Investigational agents or anticancer drugs (Including cytotoxic chemotherapy) from a previous treatment regimen or clinical study within 14 days of the first dose of study treatment
• Prior treatment with other third generation EGFR TKIs, including osimertinib, rociletinib, EGF816, olmutinib, ASP8273 and avitinib
• Brain/meninges metastases unless asymptomatic, stable and not requiring steroids for at least 4 weeks prior to start of study treatment
• History of interstitial lung disease, drug-induced interstitial lung disease, radiation pneumonitis which required steroid treatment, or any evidence of clinically active interstitial lung disease, radiological documentation of idiopathic pulmonary fibrosis at baseline; uncontrolled pleural effusion/pericardial effusion
• Any evidence of severe or uncontrolled systemic diseases, including CTCAE 2 or higher active infection, uncontrolled hypertension, unstable angina pectoris, congestive cardiac failure and severe liver/renal or metabolic disease
• Active infection including hepatitis B, hepatitis C and human immunodeficiency virus (HIV)
• History of organ transplant; had surgery or severe injury within 4 weeks
• Any clinically important abnormalities in rhythm, conduction or morphology of resting ECG eg, complete left bundle branch block, third degree heart block, second degree heart block, PR interval \>240msec, or QRS\> 110 msec
• Any factors that increase the risk of QTc prolongation or risk of arrhythmic events such as heart failure, hypokalaemia, congenital long QT syndrome, family history of long QT syndrome or unexplained sudden death under 40 years of age in first degree relatives or any concomitant medication known to prolong the QT interval
• Poorly controlled hyperglycemia(fasting blood glucose level ≥7.0 mmol/L).
• Any unresolved toxicities from prior therapy greater than Common Terminology Criteria for Adverse Events (CTCAE) grade 1 at the time of starting study treatment with the exception of alopecia
• Refractory nausea and vomiting, chronic gastrointestinal diseases, inability to swallow the formulated product or previous significant bowel resection that would preclude adequate absorption of BPI-15086

Sponsors & Collaborators

• Betta Pharmaceuticals Co., Ltd.: lead

Study Sites (1)

Department of Medical Oncology, Cancer Institute/Hospital, Chinese Academy of Medical Sciences

Beijing, Beijing Municipality, 100021, China

Location

MeSH Terms

Conditions

Carcinoma, Non-Small-Cell Lung

Condition Hierarchy (Ancestors)

Carcinoma, Bronchogenic; Bronchial Neoplasms; Lung Neoplasms; Respiratory Tract Neoplasms; Thoracic Neoplasms; Neoplasms by Site; Neoplasms; Lung Diseases; Respiratory Tract Diseases

Study Officials

• Yuankai Shi, MD

  Cancer Institute and Hospital, Chinese Academy of Medical Sciences

  STUDY CHAIR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 20, 2016
• First Posted: September 26, 2016
• Study Start: December 29, 2016
• Primary Completion: March 7, 2019
• Study Completion: March 7, 2019
• Last Updated: July 18, 2019

Record last verified: 2019-07

Data Sharing

• IPD Sharing: Will not share

Locations

CN (1)