Study Results
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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COMPLETED
20 participants
OBSERVATIONAL
2015-10-31
2018-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Eligibility Criteria
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Inclusion Criteria
2. Continuous treatment for three months with good compliance as assessed by the investigator
3. Age between 18 and 55
4. Penile-vaginal intercourse with a female partner at least twice a month with unimpeded ejaculation.
5. Compliance with safety assessments, e.g., regular bloodwork for complete blood count and liver function testing as recommended in the Package Insert
6. Able to give informed consent
Females
1. Regular sexual intercourse with a male partner who is actively taking teriflunomide
2. Age between 18 and 55
3. Able to give informed consent
4. Negative urine pregnancy test at the time of blood sampling
5. Reliable contraception that does not involve barrier methods
Exclusion Criteria
2. For males, contraindications to the continued use of teriflunomide
3. Couples that are actively trying to conceive
4. For males, noncompliance with teriflunomide therapy
5. Inability or unwilling to give consent or comply with the protocol
6. Pregnancy of the female sexual partner.
18 Years
55 Years
ALL
No
Sponsors
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Griffin Hospital
OTHER
Responsible Party
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Joseph B. Guarnaccia
Director
Principal Investigators
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Joseph Guarnaccia, MD
Role: PRINCIPAL_INVESTIGATOR
MSTC
Locations
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Multiple Sclerosis Treatment Center at Griffin Hospital
Derby, Connecticut, United States
Countries
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Other Identifiers
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TERI001
Identifier Type: -
Identifier Source: org_study_id
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