Post Marketing Surveillance Study of Cuprimine

Expanded access is no longer available for this treatment.
Information provided by (Responsible Party):
Merck Sharp & Dohme Corp. Identifier:
First received: June 14, 2011
Last updated: November 12, 2014
Last verified: November 2014

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.

Condition Intervention
Drug: Cuprimine (penicillamine)

Study Type: Expanded Access     What is Expanded Access?
Official Title: Post Marketing Surveillance Study of Cuprimine (MK-0172-001)

Resource links provided by NLM:

Further study details as provided by Merck Sharp & Dohme Corp.:

Intervention Details:
    Drug: Cuprimine (penicillamine)
    Dosage determined by the physician based on indication for treatment

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Inclusion Criteria:

- None

Exclusion Criteria:

- None

  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

No Contacts or Locations Provided
  More Information

No publications provided

Responsible Party: Merck Sharp & Dohme Corp. Identifier: NCT01374282     History of Changes
Other Study ID Numbers: 0172-001
Study First Received: June 14, 2011
Last Updated: November 12, 2014
Health Authority: Philippines: Bureau of Food and Drugs processed this record on March 31, 2015