Study of ZIO-101 in Multiple Myeloma

NCT ID: NCT00303199

Last Updated: 2012-07-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1/PHASE2

Total Enrollment

35 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-01-31

Study Completion Date

2007-08-31

Brief Summary

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The study of safety of a new organic arsenic compound in the treatment of advanced multiple myeloma

Detailed Description

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Conditions

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Multiple Myeloma

Keywords

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Multiple Myeloma Arsenic Cancer study Failed treatment

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Single Arm

Group Type EXPERIMENTAL

ZIO-101 (Darinaparsin)

Intervention Type DRUG

IV zio-101 (Darinaparsin) give for 5 consecutive days to be repeated every 28 days for up to 6 months

Interventions

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ZIO-101 (Darinaparsin)

IV zio-101 (Darinaparsin) give for 5 consecutive days to be repeated every 28 days for up to 6 months

Intervention Type DRUG

Other Intervention Names

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ZIO-101

Eligibility Criteria

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Inclusion Criteria

Subjects with multiple myeloma who have received at least two prior therapies and currently require therapy.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Alaunos Therapeutics

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Little Rock, Arkansas, United States

Site Status

West Hollywood, California, United States

Site Status

Miami, Florida, United States

Site Status

Bethesda, Maryland, United States

Site Status

New York, New York, United States

Site Status

Cleveland, Ohio, United States

Site Status

Edmonton, Alberta, Canada

Site Status

Toronto, Ontario, Canada

Site Status

Countries

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United States Canada

Other Identifiers

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SGL2001

Identifier Type: -

Identifier Source: org_study_id