Clinical Drug Experience Knowledgebase

Criteria

Inclusion criteria:

Positive diagnosis of Sjogrens syndrome, defined by meeting two or more of the following three criteria:

Positive serum anti-SS-A/Ro and/or anti-SS-B/La (or positive rheumatoid factor and ANA ≥ 1:320)
Labial salivary gland biopsy exhibiting focal lymphocytic sialadenitis with a focus score ≥ focus/4 mm2
Keratoconjunctivitis sicca with ocular staining score ≥ 3 (assuming that individual is not currently using daily eye drops for glaucoma, and has not had corneal surgery or cosmetic eyelid surgery in the last 5 years)

Or by both of the following:

Positive antibodies to one of the early markers of Sjogrens Syndrome:

Anti-salivary gland protein 1 (SP1)
Anti-carbonic anhydrase 6 (CA6)
Parotid secretory protein (PSP) Ocular staining score ≥ 3
Age ≥ 18 years at time of enrollment
Able to provide signed and dated informed consent
Women of child childbearing potential in sexual relationships with men must use an acceptable method of contraception§ from 30 days prior to enrollment until 4 weeks after completing study treatment.

Males must agree to avoid impregnation of women during and for four weeks after completing study treatment through use of an acceptable method of contraception*.

Includes, but is not limited to, barrier with additional spermicidal foam or jelly, intrauterine device, hormonal contraception (started at least 30 days prior to study enrollment), intercourse with men who underwent vasectomy.

Includes, but is not limited to, barrier with additional spermicidal foam or jelly and vasectomy.

Participant exclusion criteria

Exclusion Criteria:

Inability to provide informed consent and/or unable or unwilling to comply with protocol requirements.
Antibiotics for at least 2 weeks prior to FMT.
Active infection for >15 days: bacteremia, urinary tract infection, pneumonia or abdominal collection.
Known or suspected toxic megacolon and/or known small bowel ileus.
Previous FMT
Major gastrointestinal surgery (e.g. significant bowel resection) within 3 months before enrollment. This does not include appendectomy or cholecystectomy.
History of total colectomy or bariatric surgery.
Antibiotics for the treatment of an active infection or anticipated antibiotic use during trial duration.
Concurrent intensive induction chemotherapy, radiation therapy or biological treatment for active malignancy.
Expected life expectancy < 6 months
Patients with a history of severe anaphylactic or anaphylactoid food allergy.
Solid organ transplant patients ≤ 90 days post-transplant or on active treatment for rejection.
Neutropenia (<500 neutrophils/mL) or other severe immunosuppression. Patients on monoclonal antibodies to B and T cells, anti-tumor necrosis factor, glucocorticoids, antimetabolites, calcineurin inhibitors may be enrolled after consultation with their medical doctor.
Renal failure (GFR <30 or dialysis)
Human immunodeficiency virus+ controlled or not well controlled on antiretroviral therapy
Regular probiotic supplement use within prior 2 weeks to enrollment
Pregnancy or inability/unwillingness to use contraceptives.
A condition that would jeopardize the safety or rights of the subject, would make it unlikely for the subject to complete the study, or would confound the results of the study.
Exclusion on the discretion of the PI.