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Nanosomal Docetaxel Lipid Suspension in Treating Patients With Advanced Solid Tumors - Trial NCT01957995

Access comprehensive clinical trial information for NCT01957995 through Pure Global AI's free database. This Phase 1 trial is sponsored by University of Southern California and is currently Completed. The study focuses on Unspecified Adult Solid Tumor, Protocol Specific. Target enrollment is 13 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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NCT01957995
Phase 1
Completed
drug
Trial Details
ClinicalTrials.gov โ€ข NCT01957995
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Nanosomal Docetaxel Lipid Suspension in Treating Patients With Advanced Solid Tumors
An Open Label, Randomized Study to Evaluate Safety and Pharmacokinetics of Intravenous Infusion of Nanosomal Docetaxel Lipid Suspension for Injection in Patients With Advanced Solid Tumors

Study Focus

nanosomal docetaxel lipid suspension

Interventional

drug

Sponsor & Location

University of Southern California

Los Angeles, United States of America

Timeline & Enrollment

Phase 1

Nov 08, 2013

Jul 14, 2016

13 participants

Primary Outcome

Pharmacokinetic profile of nanosomal docetaxel lipid suspension

Summary

This randomized phase I trial studies the side effects and best dose of nanosomal docetaxel
 lipid suspension in treating patients with advanced solid tumors. Drugs used in chemotherapy,
 such as nanosomal docetaxel lipid suspension, work in different ways to stop the growth of
 tumor cells, either by killing the cells or by stopping them from dividing.

ICD-10 Classifications

Carcinoma in situ, unspecified
Malignant neoplasm, without specification of site
Malignant neoplasm, primary site unspecified
Carcinoma in situ of other and unspecified genital organs
Malignant neoplasm: Connective and soft tissue, unspecified

Data Source

ClinicalTrials.gov

NCT01957995

Non-Device Trial