A Study of BIO-11006 in the Treatment of Advanced Non-Small Cell Lung Cancer

Phase 2CompletedNCT03472053

BioMarck Pharmaceuticals, Ltd.60 enrolled

Overview

This Phase 2 is a randomized study in advanced Non-Small Cell lung cancer patients to evaluate safety and efficacy of aerosolized BIO-11006 in conjunction with chemotherapy.

This randomized, open label, multicenter Phase 2 study is to evaluate safety and efficacy of BIO-11006 in Stage IIIB Non Small Cell Lung cancer (NSCLC) patients who are not candidates for curative surgery, radiation, or immunotherapy and who are also receiving Pemetrexed and Carboplatin as standard of care (SOC). This study will be conducted at ten clinical centers in India under an IND from US-FDA and an IND from Indian FDA. This is a parallel 2- Arm study in which a total of 60 patients will be randomized. One Arm of 30 subjects will receive aerosolized 125mg BIO-11006 BID using Pari eFlow nebulizer in conjunction with SOC chemotherapy (Pemetrexed plus Carboplatin). A second Arm of 30 subjects will receive only SOC chemotherapy (Pemetrexed plus Carboplatin). The treatment period will be three months and nine months survival follow up period (every three months). Primary efficacy endpoint will be Progression-free survival (PFS) in patients who receive BIO-11006 plus SOC compared to those who receive SOC alone. The secondary efficacy endpoints will include: a. Response rate at three months (4 cycles) per RECIST V1.1; (b) overall survival; and (c) patient body weight maintenance.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

Conditions

Non Small Cell Lung Cancer Stage IIIB

Interventions

BIO-11006 plus standard of careDRUG

BIO-11006 is administered 125mg BID plus standard of care.

Standard of CareDRUG

Pemetrexed (500 mg/meter square) and Carboplatin (AUC6, Calvert's formula) are administered every three weeks for three months.

Eligibility

Sex: ALLMin age: 18 YearsMax age: 70 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. Patients who are physically able to self administer drug by nebulizer; 2. Measurable disease per RECIST Version 1.1; 3. Female patients of child bearing age must have a negative pregnancy test; 4. ECOG 0-2; 5. Written informed consent; Exclusion Criteria: 1. Candidates for curative surgery and/or radiation therapy; 2. Baseline ANC\<2000 cells/mm cube; platelet count \<100,000 cells/mm cube 3. Creatinine clearance \<45 mL/min; 4. Billirubin \>2 x the upper limit of normal 5. Known history of HIV, hepatitis B, hepatitis C or tuberculosis; 6. Current pneumonia or idiopathic pulmonary fibrosis; 7. Hypersensitivity to test drug, pemetrexed, or carboplatin.

Locations (11)

Unique Hospital and Research Institute

Surat, Gujarat, India

Aadhar Health Institute

Hisar, Haryana, India

Chirayu Cancer Hospital

Bhopal, Madhya Pradesh, India

Outcomes

Primary Outcomes

Progression-free survival

Survival period of patients in both arms of the study is measured in absence of tumor progression.

Time frame: 12 months

Secondary Outcomes

Maintenance of body weight

Patient's body weight in kilograms measured at three month and at 12 month to assess possible disease related cachexia.

Time frame: 3 and12 months

Treatment emergent adverse effects

Treatment-emergent adverse events including headache, bronchitis, dyspnea, cough, pyrexia, chest discomfort and liver function will be evaluated.

Time frame: 3 months

Data from ClinicalTrials.gov

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