A Study of RO5083945 in Combination With Cisplatin and Gemcitabine or Carboplatin and Paclitaxel in Patients With Advanced or Recurrent Non-Small Cell Lung Cancer of Squamous Histology Who Have Not Received Prior Chemotherapy for The Metastatic Disease

NCT ID: NCT01702714

Last Updated: 2016-11-04

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: PHASE1
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-07-31
• Study Completion Date: 2016-02-29

Brief Summary

This open-label, multicenter, non-randomized, dose-escalating phase Ib study with an expansion cohort will determine the recommended Phase II dose and schedule to investigate safety, tolerability, and activity of RO5083945 in combination with cisplatin and gemcitabine or carboplatin and paclitaxel in patients with advanced or recurrent non-small cell lung cancer of squamous histology who have not received prior chemotherapy for the metastatic disease. Cohorts of patients will receive escalating doses of RO5083945 in combination with up to 6 cycles of cisplatin and gemcitabine or carboplatin and paclitaxel. Anticipated time on study treatment is until disease progression or unacceptable toxicity occurs.

Conditions

Non-Squamous Non-Small Cell Lung Cancer

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

RO5083945 + carboplatin + paclitaxel

Group Type: EXPERIMENTAL

RO5083945

Intervention Type: DRUG

multiple ascending doses

carboplatin

Intervention Type: DRUG

up to 6 cycles

paclitaxel

Intervention Type: DRUG

up to 6 cycles

RO5083945 + cisplatin +gemcitabine

Group Type: EXPERIMENTAL

RO5083945

Intervention Type: DRUG

multiple ascending doses

cisplatin

Intervention Type: DRUG

up to 6 cycles

gemcitabine

Intervention Type: DRUG

up to 6 cycles

Interventions

RO5083945

multiple ascending doses

Intervention Type: DRUG

carboplatin

up to 6 cycles

Intervention Type: DRUG

cisplatin

up to 6 cycles

Intervention Type: DRUG

gemcitabine

up to 6 cycles

Intervention Type: DRUG

paclitaxel

up to 6 cycles

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Adult patients, >/= 18 years of age
• Locally advanced (stage IIIB, excluding patients who are candidates for chemo-radiotherapy or radical thoracic radiotherapy), metastatic (stage IV) or recurrent squamous non-small cell lung cancer (NSCLC)
• Histologically documented squamous NSCLC. Mixed tumors should be categorized according to the predominant cell type
• Histological tumor tissue sample from initial diagnosis or new tumor biopsy representative of the disease
• Patients who have received adjuvant chemotherapy are eligible if the last administration of the prior adjuvant regimen occurred at least 3 months prior to enrollment
• At least one measurable disease lesion as per RECIST 1.1 criteria
• Eastern Cooperative Oncology Group (ECOG) performance status 0-1
• Adequate hematological, liver and renal function
• Females of childbearing potential must commit to using a reliable and appropriate method of contraception until at least 3 months after the end of the last dose of study treatment

Exclusion Criteria

• Prior chemotherapy (excluding neoadjuvant/adjuvant chemotherapy/chemo-radiotherapy) or treatment with another systemic anti-cancer agent (e.g. monoclonal antibody, tyrosine kinase inhibitor)
• Radiotherapy within the last 4 weeks prior to first dosing, except for limited field palliative radiotherapy for bone pain relief
• Treatment with any other investigational agent within 30 days prior to starting study treatment or participation in another clinical trial (e.g. CTC blood collection) within 7 days prior to starting study treatment
• Historical or clinical evidence of central nervous system (CNS) metastases (except for previously treated CNS metastases in patients that are asymptomatic, have had no evidence of active CNS metastases for >/= 3 months prior to first dose and have had no requirement for steroids or enzyme-inducing anticonvulsants in the last 14 days)
• Recent history of poorly controlled hypertension (systolic >180 mmHg or diastolic >100 mmHg)
• Severe uncontrolled illness, including poorly controlled diabetes mellitus and active or uncontrolled infection
• Hypersensitivity to the active substance or to any excipients or to any of the study drugs including premedication (corticosteroids, anti-histamine, paracetamol)
• Pregnant or breastfeeding women

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Hoffmann-La Roche

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Clinical Trials

Role: STUDY_DIRECTOR

Hoffmann-La Roche

Other Identifiers

2012-003376-39

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

BP28577

Identifier Type: -

Identifier Source: org_study_id