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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00040547
Other study ID # P01964
Secondary ID
Status Completed
Phase Phase 1
First received June 28, 2002
Last updated February 16, 2015
Start date June 2001
Est. completion date February 2004

Study information

Verified date February 2015
Source Merck Sharp & Dohme Corp.
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the safety and tolerability of an oral Farnesyl Protein Transferase Inhibitor (SCH 66336) when given in combination with intravenous docetaxel in cancer patients with advanced solid tumors.


Recruitment information / eligibility

Status Completed
Enrollment 29
Est. completion date February 2004
Est. primary completion date February 2004
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion:

- Male or Female

- Measurable or evaluable disease

- No more than 2 prior chemotherapy regimens.

- Age greater than or equal to 18.

- Karnofsky Performance Status greater than or equal to 70%.

- Meets protocol requirements for specified laboratory values.

- No manifestations of a malabsorption syndrome.

- Written informed consent and cooperation of patient

- Appropriate use of effective contraception if of child-bearing potential.

Exclusion:

- Acute or chronic leukemia or multiple myeloma.

- Evidence of 2 or more active malignancies, expect for in situ or adequately treated basal or squamous cell skin cancer.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Farnesyl Protein Transferase Inhibitor


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Merck Sharp & Dohme Corp.

Outcome

Type Measure Description Time frame Safety issue
Primary Adverse Events
Primary Laboratory Tests
Primary ECG
Secondary Physical Exam
Secondary Pharmacokinetics
Secondary Tumor Response
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