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Phase I Study of Indibulin in Patients With Solid Tumors

Phase 1
Completed
Conditions
Solid Tumors
Interventions
Registration Number
NCT00591136
Lead Sponsor
Alaunos Therapeutics
Brief Summary

Dose-finding and pharmacokinetic trial of orally administered Indibulin to patients with solid tumors.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
47
Inclusion Criteria

Not provided

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Exclusion Criteria

Not provided

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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Single Armindibulin-
Primary Outcome Measures
NameTimeMethod
toxicities4 months
Secondary Outcome Measures
NameTimeMethod
pharmacokinetics4 months
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