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Clinical Trial for metastatic melanoma patients.(skin cancer)

Phase 3
Completed
Conditions
Health Condition 1: null- Patients with histologically confirmed metastatic melanomaharboring the BRAF V600 mutation as determined by the cobas® 4800 BRAF V600 Mutation Test.
Registration Number
CTRI/2012/07/002756
Lead Sponsor
Roche Products India Pvt Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
900
Inclusion Criteria

Inclusion Criteria:

1. Male or female patients >= 16 years of age

2. Patients with histologically confirmed

metastatic melanoma (surgically incurable

and unresectable stage IIIC or stage IV;

AJCC) with documented BRAF V600 mutation

determined by the cobas® 4800 BRAF V600

Mutation Test prior to administration of

RO5185426. Unresectable stage IIIC disease

must have confirmation from a surgical

oncologist

3. Patients with either measurable or non-

measurable disease(RECIST Version 1.1)

4. Patients may or may not have received prior

systemic therapy for metastatic melanoma

5. Eastern Cooperative Oncology Group (ECOG)

performance status (PS) of 0-2

6. Patients must have recovered from all side

effects of their most recent systemic or

local treatment for metastatic melanoma

7. Adequate hematologic, renal and liver

function as defined by the following

laboratory values performed within 7 days

prior to first dose of RO5185426:

• Absolute neutrophil count (ANC) >= 1.5 x

109/L

• Platelet count >= 100 x 109/L

• Hemoglobin >= 9 g/dL

• Serum creatinine <= 1.5 times upper limit

of normal (ULN) or creatine clearance

(CrCl) > 50 mL/hr by Cockroftâ??Gault formula

• Aspartate aminotransferase (AST [SGOT]) and

alanine aminotransferase (ALT [SGPT]) <= 2.5

times ULN (<= 5times ULN if considered due

to tumor)

• Serum bilirubin <= 1.5 times ULN

• Alkaline phosphatase <= 2.5 times ULN (<=

5times ULN if considered due to tumor)

8. Negative serum pregnancy test within 7 days

prior to commencement of dosing in

premenopausal women. Women of non-

childbearing potential may be included if

they are either surgically sterile or have

been postmenopausal for >=1 year.

9. Fertile men and women must use an effective

method of contraception during treatment and

for at least 6 months after completion of

treatment as directed by their physician.

Effective methods of contraception are

defined as those which result in a low

failure rate (i.e. less than 1% per year) when

used consistently and correctly (for example

implants, injectables, combined oral

contraception or intra-uterine devices). At

the discretion of the investigator, acceptable

methods of contraception may include total

abstinence in cases where the lifestyle of

the patient ensures compliance.[Periodic

abstinence (e.g. calendar, ovulation,

symptothermal, postovulation methods) and

withdrawal are not acceptable methods of

contraception.]

10.Absence of any psychological, familial,

sociological or geographical condition

potentially hampering compliance with the

study protocol and follow-up schedule; those

conditions should be discussed with the

patient before trial entry

11.Signed informed consent must be obtained

prior to performing any study-related

procedures (includ

Exclusion Criteria

1. Evidence of symptomatic CNS lesions as

determined by investigator (patients with

radiographically stable, asymptomatic lesions

previously irradiated or surgically resected

are eligible)

2. Patients with a previous malignancy (other

than melanoma) within the past 2 years are

excluded except patients with treated and

controlled basal or squamous cell carcinoma

(SCC) of the skin or carcinoma in-situ of the

cervix. Isolated elevation in prostate-

specific antigen in absence of radiographic

evidence of metastatic prostate cancer is

allowed

3. Concurrent administration of any anti-cancer

therapies (e.g. chemotherapy, other targeted

therapy, experimental drug, etc) other than

those administered in this study

4. Known hypersensitivity to RO5185426 or

another BRAF inhibitor

5. Pregnant or lactating women

6. Refractory nausea and vomiting,malabsorption,

external biliary shunt, or significant bowel

resection that would preclude adequate

absorption. Patients must be able to swallow

tablets

7. Any of the following within the 6 months

prior to first RO5185426 administration:

myocardial infarction, severe/unstable

angina, symptomatic congestive heart failure,

cerebrovascular accident or transient

ischemic attack, pulmonary embolism,

hypertension not adequately controlled

by current medications

8. History of congenital long QT syndrome,

history or presence of clinically significant

ventricular or atrial dysrhythmias >= Grade 2

(NCI CTCAE Version 4.0)

9. Corrected QT (QTc) interval >= 450 msec at

baseline

10.Uncontrolled medical illness (such as

infection requiring treatment with

intravenous (IV) antibiotics)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate the safety and tolerability of RO5185426 in <br/ ><br>patients with metastatic melanoma (surgically incurable and <br/ ><br>unresectable stage IIIC or stage IV; AJCC) harboring the BRAF V600 mutation.Timepoint: N/A
Secondary Outcome Measures
NameTimeMethod
To evaluate the efficacy of RO5185426 as overall <br/ ><br>response rates (ORRs) determined by the investigator (RECIST, <br/ ><br>Version 1.1) as allowed by local regulatory requirements.Timepoint: Screening, Cycle 3, Cycle 5 and End of the study.
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