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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02679885
Other study ID # TERI001
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 2015
Est. completion date September 2018

Study information

Verified date December 2018
Source Griffin Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

It is known that teriflunomide, a treatment for relapsing forms of multiple sclerosis, can be found in low concentrations in semen. Because the drug has been associated with teratogenicity in laboratory animals, the question is raised as to whether the drug can be detected in female partners of sexually active males who are taking the drug to treat their multiple sclerosis.


Description:

A total of 10 couples were enrolled in the study. Females partners had undetectable or borderline levels of teriflunomide.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date September 2018
Est. primary completion date August 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria:

1. Males with relapsing forms of multiple sclerosis appropriately treated with teriflunomide 14 mg po daily;

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:

1. Use of barrier methods of contraception

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.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Multiple Sclerosis Treatment Center at Griffin Hospital Derby Connecticut

Sponsors (1)

Lead Sponsor Collaborator
Griffin Hospital

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Serum levels of teriflunomide in males and their female partners single laboratory evaluation Up to one year
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