Pomalidomide in Hereditary Hemorrhagic Telangiectasia and Transfusion-Dependent Vascular Ectasia: a Phase I Study

This is a single-arm, open-label study that will investigate the efficacy and safety profile
of pomalidomide in patients with genetically-documented Hereditary Hemorrhagic Telangiectasia
(defined by characteristic mutations in Eng, Alk-1 or Smad-4) or idiopathic vascular ectasia
with no documented mutations, leading to refractory bleeding of the small bowel. This study
will be limited to patients with documented bleeding from the small bowel, including the
duodenum, jejunum or ileum. Eligible patients will be dependent on transfusion or intravenous
iron therapy (requiring at least 4 units of blood transfusion or 4 iron infusions over the
preceding 4 months) and will have endoscopically-confirmed areas of vascular ecstasia.
Therapy for all eligible patients will be initiated with a 1 mg daily dose of pomalidomide.
The principal investigator will determine whether intrapatient dose escalation is indicated
based on the response of the patient's bleeding during the first 30 days of therapy. If dose
escalation is indicated, pomalidomide will be increased at the investigator's discretion to a
maximal dose of 5 mg/day. Cessation of GI bleeding will be defined as maintenance of stable
hemoglobin without blood transfusion or intravenous iron therapy over a 4 week period. Once
GI bleeding has ceased, patients will be maintained at a stable pomalidomide dose for an
additional 4 months, and the dose then tapered by 1 mg per month, or until bleeding recurs.
Patients will be followed for a total of six months post-therapy to determine whether the
response is maintained.

Inclusion Criteria:

1. Age > 18 years

2. Transfusion of at least 4 units of blood and/or four doses of intravenous iron over
the preceding four months.

3. Recurrent bleeding after at least one previous interventional endoscopic procedure

4. Platelet count ≥ 125,000/µl

5. WBC ≥ 4,000/µl

6. Normal prothrombin (PT) and activated partial thromboplastin time (aPTT)

7. Endoscopically-documented angiodysplasia and/or arteriovenous malformations involving
the small bowel

8. Females of childbearing potential (FCBP)† must have a negative serum or urine
pregnancy test with a sensitivity of at least 25 mIU/mL within 10 - 14 days prior to
and again within 24 hours of prescribing pomalidomide and must either commit to
continued abstinence from heterosexual intercourse or begin TWO acceptable methods of
birth control, one highly effective method and one additional effective method AT THE
SAME TIME, at least 28 days before she starts taking pomalidomide. FCBP must also
agree to ongoing pregnancy testing. Men must agree to use a latex condom during sexual
contact with a FCBP even if they have had a vasectomy.

9. Ability to understand and sign informed consent

10. All study participants must be registered into the mandatory POMALYST REMS™ program,
and be willing and able to comply with the requirements of the POMALYST REMS™ program

Exclusion Criteria:

1. Pregnancy (must be excluded by two urine or serum tests for β-HCG in all women of
child-bearing potential).

Pregnancy Testing -Must follow pregnancy testing requirements as outlined in the
POMALYST REMS™ program.

2. Breast feeding

3. Renal insufficiency, serum creatinine > 2.0 mg/dl

4. Hepatic insufficiency, bilirubin > 2.0 or transaminases > 3.0 x normal

5. Previous treatment with Thalidomide or other imid drugs within previous 12 months

6. History of prior thromboembolism with known thrombophilia

7. Peripheral neuropathy, as determined from neurologic consultation

8. Underlying hypoproliferative anemia (i.e. myelodysplasia)

9. Inherited or significant acquired coagulopathy (i.e. hemophilia, advanced liver
disease)

10. Chronic aspirin, NSAID therapy, anticoagulation therapy or antiplatelet agents

11. Currently enrolled in other interventional trials

12. Known hypersensitivity to thalidomide or lenalidomide.

13. The development of erythema nodosum if characterized by a desquamating rash while
taking thalidomide, or similar drugs.

14. Anything that in the investigator's opinion is likely to interfere with completion of
the study † A female of childbearing potential is a sexually mature woman who: 1) has
not undergone a hysterectomy or bilateral oophorectomy; or 2) has not been naturally
postmenopausal for at least 24 consecutive months (i.e., has had menses at any time in
the preceding 24 consecutive months).