Overview

Teduglutide for Enterocutaneous Fistula (ECF)

Status:
Completed
Trial end date:
2021-07-15
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to determine whether Teduglutide is safe and feasible to be given for the treatment of enterocutaneous fistula (ECF). The hypothesis is that the drug will be well tolerated and will improve the volume of daily ECF output as well as improve the functional quality of life.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Daniel Dante Yeh
Massachusetts General Hospital
Collaborator:
Takeda
Treatments:
Teduglutide
Criteria
Inclusion Criteria:

- Age >18

- Enterocutaneous fistula (ECF) that could be secondary to volvulus, injury, prior
trauma or surgery, or vascular ischemia

Exclusion Criteria:

- Perianal fistula

- Clinical suspicion of inflammatory bowel disease

- History of radiation enteritis or sprue (as defined by history)

- Active (<1 year) alcohol or drug abuse

- Significant hepatic, or cardiac diseases as defined as:

- Hepatic: aspartate aminotransferase (AST) > 2 times upper limit of normal (10-40 U/L)

- Cardiac: unstable angina or evidence of active myocardial ischemia (elevated troponin
level drawn by clinical suspicion)

- Severe renal dysfunction: serum creatinine > 2 times upper limit of normal (0.6-1.5
mg/dL)

- Received glutamine less than 4 weeks prior to screening

- Receiving growth factors (erythropoietin, granulocyte colony-stimulating factor,
granulo-cyte-macrophage colony stimulating factor, and human growth hormone)

- Pregnancy or lactation (women of childbearing age will be excluded if they do not
agree to either complete sexual abstinence during the study or if they refuse to use
at least two forms of highly effective contraception such as oral contraception,
injectable or implantable contraception, vaginal rings, or intrauterine devices (IUD))

- Active malignancy or suspicion for gastrointestinal malignancy on CT scan

- Not capable of understanding or not willing to adhere to the study visit schedule and
drug administration requirements

- Family history of intestinal malignancy (gastric, small intestine, colon)

- Personal or family history of hereditary non-polyposis colorectal cancer, familial
adenomatous polyposis, first degree relative with colon cancer

- Positive hemoccult (per rectum)

- Abnormal baseline electrocardiogram (ECF) suggestive of congestive heart failure or
underlying cardiac disease

- Taking oral benzodiazepines, barbiturates, or phenothiazines