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Study of Filgotinib to assess the Safety and Efficacy in Subjects with Rheumatoid Arthritis

Phase 3
Conditions
Health Condition 1: M058- Other rheumatoid arthritis with rheumatoid factorHealth Condition 2: null- Patients with RheumatoidArthritis
Registration Number
CTRI/2018/12/016581
Lead Sponsor
Galapagos NV
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Closed to Recruitment of Participants
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Able and willing to sign the informed consent as approved by the IRB/IEC. Written consent

must be provided before initiating any Day -1 evaluations for this study. Subjects must have

read and understood the ICF, must fully understand the requirements of the study, and must

be willing to comply with all study visits and assessments; subjects who cannot read or

understand the ICF may not be enrolled by a guardian or any other individual.

2. Male or female subjects who may benefit from filgotinib as judged by the investigator AND

who completed a Gilead sponsored filgotinib parent study for RA as outlined below:

a) Subjects who completed GS-US-417-0301, GS-US-417-0302, GS-US-417-0303 or

GS-US-417-3910 on study drug

OR

b) Subjects who completed GS-US-417-0302 on standard of care therapy due to RA

non-responder status

OR

c) Subjects who completed GS-US-417-3910 on standard of care therapy due to

semen-related stopping criteria

3. Females of childbearing potential must have a negative pregnancy test at Day -1 and must

agree to continued monthly pregnancy testing during the study

4. Lactating female subjects must agree to discontinue nursing at Day -1 for the duration of the

study

5. Male and female subjects of childbearing potential who engage in heterosexual intercourse

must agree to use protocol specified method(s) of contraception as described in Appendix 5,

during the study and through 35 days (female) or 90 days (male) after their last dose of study

drug.

6. Subjects receiving protocol permitted RA medications should be on a stable dose (defined as

no change in prescription) within 7 days or 5 half-lives (whichever is longer) prior to the

first administration of study drug on Day 1.

Note: Subjects on MTX during their parent study will have their MTX dose discontinued at the

time of Day -1 and be evaluated for resuming of MTX treatment after 4 weeks of study drug

treatment on the LTE study.

7. Subjects, who meet study drug interruption criteria (as outlined in Section 3.5.1) at Day -1,

are eligible to enter into the LTE, but should not start study drug until deemed medically

appropriate. Study drug should be reinitiated as outlined in Section 3.5.1.

Exclusion Criteria

Subjects who meet any of the following are not to be enrolled in this study.

1) An autoimmune or inflammatory joint disease other than RA, which would put the subject at

risk by participating in the study or would interfere with study assessments/data

interpretation, per judgment of the investigator; (Sjogren’s syndrome or stable thyroiditis is

permitted).

2) Known hypersensitivity to the study drug, its metabolites or formulation excipients.

3) Any medical condition (including, but not limited to, cardiac or pulmonary disease, alcohol

or drug abuse) which would put the subject at risk by participating in the study or would

interfere with study assessments/data interpretation, per judgment of the investigator;

4) Administration of a live/ attenuated vaccine within 30 days prior to Day -1

5) Currently on any therapy for chronic infection (such as pneumocystis, cytomegalovirus,

herpes zoster, and atypical mycobacteria)

6) History of disseminated/complicated herpes zoster infection (multi-dermatomal involvement,

ophthalmic zoster, central nervous system involvement or postherpetic neuralgia)

7) Any condition or circumstances which in the opinion of the investigator or Sponsor may

make a subject unlikely or unable to complete the study or comply with study procedures and

requirements

8) Use of prohibited medication as outlined in Section 5.4

9) Subjects who meet discontinuation criteria as outlined in outlined in Section 3.5.2

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate the long-term safety and tolerability of filgotinib in <br/ ><br>subjects who have completed one of the parent studies of filgotinib <br/ ><br>in RATimepoint: 6 years
Secondary Outcome Measures
NameTimeMethod
To evaluate the long-term safety and tolerability of filgotinib in <br/ ><br>subjects who have completed one of the parent studies of filgotinib <br/ ><br>in RATimepoint: 6 years
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