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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01363947
Other study ID # DNB4987g
Secondary ID GO277672014-0005
Status Completed
Phase Phase 1
First received May 26, 2011
Last updated June 5, 2017
Start date June 14, 2011
Est. completion date June 3, 2016

Study information

Verified date June 2017
Source Genentech, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Study DNB4987g is a Phase I, multicenter, open label, dose-escalation study of DNIB0600A administered as a single agent by intravenous (IV) infusion every three weeks (q3w) to participants with non-squamous NSCLC or non-mucinous, platinum-resistant ovarian cancer. The study will be conducted in two cohorts: Dose-escalation cohort and Expansion cohort.


Recruitment information / eligibility

Status Completed
Enrollment 87
Est. completion date June 3, 2016
Est. primary completion date June 3, 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1

- Histologic documentation of incurable, locally advanced or metastatic disease that has failed prior chemotherapy and for which no standard therapy exists, including the following: non-squamous NSCLC or non-mucinous and platinum-resistant ovarian cancer

- Availability and willingness to provide an adequate archival sample of tumor

- Measurable disease

- For fertile men or women of childbearing potential, documented willingness to use a highly effective means of contraception

Exclusion Criteria:

- Anti-tumor therapy, including chemotherapy, biologic, experimental, or hormonal therapy within 4 weeks prior to study treatment

- Major surgical procedure within 4 weeks prior to study treatment

- Known active bacterial, viral, fungal, mycobacterial, or other infection (including human immunodeficiency virus [HIV] and atypical mycobacterial disease, but excluding fungal infections of the nail beds)

- Clinically significant history of liver disease, including viral or other hepatitis, current alcohol abuse, or cirrhosis

- Untreated or active central nervous system (CNS) metastases

- Requirement for supplemental oxygen to carry out activities of daily living

- Any other diseases, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicates the use of an investigational drug or that may affect the interpretation of the results or render the participant at high risk from treatment complications

- Evidence of significant uncontrolled concomitant diseases, such as cardiovascular disease, nervous system, pulmonary, renal, hepatic, endocrine, or gastrointestinal disorders; or a serious non-healing wound or fracture

- For participants in the second NSCLC cohort expansion, not more than two prior regimens in the metastatic setting

- Pregnancy or breast-feeding

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
DNIB0600A
Several dose levels will be evaluated for DNIB0600A administered via IV infusion on Day 1 of each 21-day cycle until disease progression.

Locations

Country Name City State
Spain Hospital del Mar; Servicio de Oncologia Barcelona
Spain Hospital Univ Vall d'Hebron; Servicio de Oncologia Barcelona
Spain Hospital General Universitario Gregorio Marañon; Servicio de Oncologia Madrid
United States Univ of Texas SW Medical Ctr Dallas Texas
United States Sarah Cannon Research Inst. Nashville Tennessee
United States Smilow Cancer Hospital at Yale New Haven New Haven Connecticut
United States HonorHealth Research Institute - Pima Center Scottsdale Arizona

Sponsors (1)

Lead Sponsor Collaborator
Genentech, Inc.

Countries where clinical trial is conducted

United States,  Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of Participants With Adverse Events (AEs) An AE is defined as any unfavorable and unintended sign, symptom, or disease temporally associated with the use of an investigational medicinal product (IMP) or other protocol-imposed intervention, regardless of causality. Up to approximately 2 years
Secondary Cmax of DNIB0600A for Antibody-Conjugated Monomethyl Auristatin E (acMMAE), Total Antibody, and Unconjugated Monomethyl Auristatin E (MMAE) Cmax is the peak concentration of a substance in blood serum. Day 21
Secondary Percentage of Participants with Antibody Formation to DNIB0600A Serum samples will be analyzed to assess the prevalence of anti-drug antibodies (ADAs) at baseline and the incidence of post-baseline ADAs in each treatment group. Up to approximately 84 weeks
Secondary Percentage of Participants with Objective Response (OR) OR is defined as a complete or partial response according to the Response Evaluation Criteria in Solid Tumors (RECIST), v1.1. Complete response is defined as disappearance of all target lesions. Partial response is defined as at least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum of diameters. Stable disease is defined as neither sufficient shrinkage to qualify for partial response nor sufficient increase to qualify for progressive disease, taking as reference the smallest sum on study. Progressive disease is defined as at least a 20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study, including baseline. In addition to the relative increase of 20%, the sum must also demonstrate an absolute increase of at least 5 millimeters (mm). The appearance of one or more new lesions is also considered progression. Up to approximately 84 weeks
Secondary Duration of Objective Response (DOR) OR is defined as a complete or partial response according to the Response Evaluation Criteria in Solid Tumors (RECIST), v1.1. Complete response is defined as disappearance of all target lesions. Partial response is defined as at least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum of diameters. Stable disease is defined as neither sufficient shrinkage to qualify for partial response nor sufficient increase to qualify for progressive disease, taking as reference the smallest sum on study. Progressive disease is defined as at least a 20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study, including baseline. In addition to the relative increase of 20%, the sum must also demonstrate an absolute increase of at least 5 millimeters (mm). The appearance of one or more new lesions is also considered progression. Up to approximately 84 weeks