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

December 22, 2022 updated by: Eiger BioPharmaceuticals

Ubenimex in Adult Patients With Lymphedema of The Lower Limb: a Phase 2, RAndomized, Double-blind, Placebo-controlled Study of Efficacy, Safety, and Pharmacokinetics (ULTRA)

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.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

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

Study Type

Interventional

Enrollment (Actual)

54

Phase

  • Phase 2

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • New South Wales
      • Sydney, New South Wales, Australia, 2109
        • Macquarie University Hospital (MUH)
    • California
      • Stanford, California, United States, 94305
        • Stanford University
    • Florida
      • Orlando, Florida, United States, 32806
        • Orlando Health, Inc.
    • Ohio
      • Columbus, Ohio, United States, 43210
        • The Ohio State University Wexner Medical Center James Cancer Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 75 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. 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.
  2. Swelling of at least 1 leg not completely reversed by leg elevation or compression.
  3. Stage II or greater lymphedema, based on the International Society of Lymphology (ISL) staging system.
  4. Completion of a full course of complete decongestive therapy (CDT).
  5. Stable limb volume (within 10% during screening for worse/affected leg) .
  6. 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.
  7. Ambulatory status (use of a walking aid is permitted).
  8. Agree to use a medically acceptable method of contraception, if the possibility of conception exists.

Exclusion Criteria:

Exclusions Based on Lymphedema:

  1. 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)
  2. Occurrence of significant lymphedema of another body part that is not the lower limb (e.g, upper extremity, trunk, head and neck, genitalia).
  3. Lymphedema involving all four limbs
  4. Recent initiation of, or intention to initiate CDT or maintenance physiotherapy for lymphedema.

    Exclusions Based on Other Medical Conditions

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

    Exclusions Based on Concurrent Medication Use

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

    Exclusions Based on Laboratory Values

  22. Significant or chronic renal insufficiency or requires dialytic support.
  23. Hepatic dysfunction.
  24. Absolute neutrophil count <1500 mm3 at screening.
  25. Hemoglobin concentration <9 g/dL at screening.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Quadruple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: ubenimex
ubenimex capsules 150 mg three times a day (TID), administered orally for a total of 24 weeks.
Other Names:
  • UBX
Placebo Comparator: placebo
matched placebo capsules TID, administered orally for a total of 24 weeks

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Skin Thickness of the Calf of the Most Affected Leg, Measured by Skinfold Calipers
Time Frame: 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).
Baseline through Week 24

Secondary Outcome Measures

Outcome Measure
Time Frame
Change in lymphedema-specific patient reported outcome measures (Patient-Reported Evaluation of Lymphedema [Leg]) questionnaire results
Time Frame: Week 24
Week 24
Change in leg volume of the most affected leg
Time Frame: Week 24
Week 24
Change in extracellular fluid volume of the lower limb, measured by the bioimpedance spectroscopy device.
Time Frame: Week 24
Week 24
Change in biospy result for dermal thickness
Time Frame: Week 24
Week 24

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

June 1, 2016

Primary Completion (Actual)

October 1, 2018

Study Completion (Actual)

February 1, 2019

Study Registration Dates

First Submitted

February 26, 2016

First Submitted That Met QC Criteria

March 2, 2016

First Posted (Estimate)

March 7, 2016

Study Record Updates

Last Update Posted (Actual)

January 18, 2023

Last Update Submitted That Met QC Criteria

December 22, 2022

Last Verified

December 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • EIG-UBX-003

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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