Ubenimex in Adult Patients With Lymphedema of The Lower Limb (ULTRA)

Phase 2

Completed

Conditions: Lymphedema

Interventions: Other: placebo
Drug: ubenimex

Registration Number: NCT02700529

Lead Sponsor: Eiger BioPharmaceuticals

Brief Summary: This proof-of-concept study is designed as a randomized, double-blind, placebo-controlled study comparing ubenimex at 150 mg, 3 times daily (total daily dose of 450 mg) with placebo for 6 months treatment period in patients with leg lymphedema.

Detailed Description: Leukotriene B4 (LTB4) inhibits lymphangiogenesis in the mouse tail model of lymphedema and is elevated in tissue in patients with lymphedema. Ubenimex is an inhibitor of leukotriene A4 hydrolase (LTA4H), the biosynthetic enzyme for LTB4. This proof-of-concept study is designed as a randomized, double-blind, placebo-controlled study comparing ubenimex at 150 mg, 3 times daily (total daily dose of 450 mg) with placebo for 6 months treatment period in patients with leg lymphedema. The primary objectives for the study are:

* To evaluate the efficacy of ubenimex in patients with leg lymphedema

* To evaluate the safety and tolerability of ubenimex in patients with leg lymphedema

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 54

Inclusion Criteria

Has a diagnosis of secondary leg lymphedema, based on a positive lymphoscintigraphy (LSG) study of the affected leg OR has a diagnosis of primary lymphedema not of congenital onset affecting one or both lower limbs, based on positive LSG.
Swelling of at least 1 leg not completely reversed by leg elevation or compression.
Stage II or greater lymphedema, based on the International Society of Lymphology (ISL) staging system.
Completion of a full course of complete decongestive therapy (CDT).
Stable limb volume (within 10% during screening for worse/affected leg) .
If patient has had a lymphatic vascularization procedure (lymphovenous bypass or lymph node transfer) or liposuction for lymphedema in the affected limb, then procedure must have been performed at least 1 year (12 months) prior to Screening AND affected limb must be clinically stable over the 3 months prior to Screening AND significant residual disease must be present.
Ambulatory status (use of a walking aid is permitted).
Agree to use a medically acceptable method of contraception, if the possibility of conception exists.

Exclusion Criteria

Exclusions Based on Lymphedema:

A diagnosis of primary lymphedema with congenital onset. Primary lymphedema is defined as lymphedema with onset prior to or without an inciting event (e.g, surgery, trauma, radiation)
Occurrence of significant lymphedema of another body part that is not the lower limb (e.g, upper extremity, trunk, head and neck, genitalia).
Lymphedema involving all four limbs
Recent initiation of, or intention to initiate CDT or maintenance physiotherapy for lymphedema.

Exclusions Based on Other Medical Conditions
Deep venous thrombosis in either lower limb or systemic anticoagulation within 6 months
Other medical condition that could lead to acute or chronic leg edema.
Other medical condition that could result in symptoms overlapping those of lymphedema in the affected leg.
History of clotting disorder (hypercoagulable state).
Chronic (persistent) infection in either lower limb.
Cellulitis or other infection in either lower limb or use of antibiotics for cellulitis within 3 months prior to screening.
Other unstable or severe medical condition requiring active management and/or likely to decompensate/require active management within the next year
Current evidence of malignancy.
History of malignancy within the previous 3 years, except for nonmelanoma skin cancer or cervical carcinoma in situ treated with curative intent.
Currently receiving chemotherapy or radiation therapy.
Life expectancy < 2 years for any reason.
Pregnancy or nursing.
Substance abuse (such as alcohol or drug abuse) within 6 months prior to screening.

Exclusions Based on Concurrent Medication Use
Regular concurrent use or regular use within 6 months before screening of another leukotriene pathway inhibitor.
Concurrent antibiotic use.
Concurrent use of any agent active on the sphingosine-1-phosphate (S1P) pathway.
Concurrent use of unapproved (including herbal) treatments for lymphedema.

Exclusions Based on Laboratory Values
Significant or chronic renal insufficiency or requires dialytic support.
Hepatic dysfunction.
Absolute neutrophil count <1500 mm3 at screening.
Hemoglobin concentration <9 g/dL at screening.

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
placebo	placebo	matched placebo capsules TID, administered orally for a total of 24 weeks
ubenimex	ubenimex	ubenimex capsules 150 mg three times a day (TID), administered orally for a total of 24 weeks.

Primary Outcome Measures

Name	Time	Method
Change in Skin Thickness of the Calf of the Most Affected Leg, Measured by Skinfold Calipers	Baseline through Week 24	Change from baseline to Week 24 in skin thickness of the calf of the most affected leg, measured by skinfold calipers in the Skin-Thickness Intent-to-Treat (ST-ITT) population (patients with skin thickness \>/= 10 mm at baseline) which comprised of 36 patients (16 ubenimex, 20 placebo).

Secondary Outcome Measures

Name	Time	Method

Trial Locations

Locations (4): Stanford University
🇺🇸
Stanford, California, United States
Orlando Health, Inc.
🇺🇸
Orlando, Florida, United States
The Ohio State University Wexner Medical Center James Cancer Hospital
🇺🇸
Columbus, Ohio, United States
Macquarie University Hospital (MUH)
🇦🇺
Sydney, New South Wales, Australia
Stanford University
🇺🇸Stanford, California, United States