Scleroderma Clinical Trial
Official title:
Post Marketing Surveillance Study of Cuprimine (MK-0172-001)
NCT number | NCT01374282 |
Other study ID # | 0172-001 |
Secondary ID | |
Status | No longer available |
Phase | N/A |
First received | June 14, 2011 |
Last updated | October 21, 2015 |
Verified date | October 2015 |
Source | Merck Sharp & Dohme Corp. |
Contact | n/a |
Is FDA regulated | No |
Health authority | Philippines: Bureau of Food and Drugs |
Study type | Expanded Access |
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.
Status | No longer available |
Enrollment | 0 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A and older |
Eligibility |
Inclusion Criteria: - None Exclusion Criteria: - None |
N/A
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Merck Sharp & Dohme Corp. |
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