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NCT03123029 Clinical Trial

Expanded Access to Venetoclax

Multiple Myeloma Clinical Trial

Official title:
Expanded Access to Venetoclax

Clinical Trial Details — Status: Available

Administrative data
NCT number NCT03123029
Other study ID # C16-431
Secondary ID C19-920
Status Available
Phase
First received
Last updated

Study information
Verified date April 2024
Source AbbVie
Contact ABBVIE CALL CENTER
Phone 844-663-3742
Email abbvieclinicaltrials@abbvie.com
Is FDA regulated No
Health authority
Study type Expanded Access

Clinical Trial Summary

This is an expanded access program (EAP) for eligible participants. This program is designed to provide access to Venetoclax prior to approval by the local regulatory agency. Availability will depend on territory eligibility. A medical doctor must decide whether the potential benefit outweighs the risk of receiving an investigational therapy based on the individual patient's medical history and program eligibility criteria.

Recruitment information / eligibility
Status Available
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - The participant must not be eligible for a venetoclax clinical trial. - Pediatric participants may be evaluated on a case by case basis.

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Venetoclax
Venetoclax will be administered orally.

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
AbbVie
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