Post Marketing Surveillance Study of Cuprimine

NCT ID: NCT01374282

Last Updated: 2015-10-22

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

NO_LONGER_AVAILABLE

Study Classification

EXPANDED_ACCESS

Brief Summary

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Cuprimine (penicillamine) was made available in the Philippines by the Sponsor under a Compassionate Special Permit issued by the Bureau of Food and Drugs. Physicians were able to request the drug for their patients from the Sponsor. A Clinical Study Report form was completed for each purchase of Cuprimine.

Detailed Description

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Conditions

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Scleroderma

Interventions

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Cuprimine (penicillamine)

Dosage determined by the physician based on indication for treatment

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

\- None

Exclusion Criteria

\- None
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Merck Sharp & Dohme LLC

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Other Identifiers

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0172-001

Identifier Type: -

Identifier Source: org_study_id

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