Title

Pegtibatinase as an Enzyme Therapy for Patients With Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency (COMPOSE)
A Double Blind, Randomized, Placebo-controlled, Phase 1/2 Study to Assess the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Effects on Clinical Outcomes of Pegtibatinase (TVT-058), Administered Subcutaneously in Patients With Cystathionine Beta-Synthase Deficient Homocystinuria (COMPOSE)
  • Phase

    Phase 1/Phase 2
  • Study Type

    Interventional
  • Status

    Recruiting
  • Intervention/Treatment

    ot-58 ...
  • Study Participants

    32
Homocystinuria caused by Cystathionine Beta-Synthase (CBS) Deficiency is a rare autosomal-recessive metabolic condition characterized by an excess of homocysteine (Hcy) in the plasma, tissues and urine. It is due to reduced or absent activity of the CBS enzyme, and is also known as classical homocystinuria. The symptoms associated with homocystinuria are variable in severity and time of onset across patients. Some affected individuals may have mild signs of the disorder; others may have multi-systemic involvement including potentially life-threatening complications. Homocystinuria can affect many different organ systems of the body; the four most commonly involved are the eyes, central nervous system, skeleton, and the vascular system.

The current approaches to treatment of homocystinuria patients include a highly restrictive diet and use of dietary supplements. Lifetime compliance with this diet is poor. Pegtibatinase (TVT-058) represents a novel therapeutic approach that incorporates the use of a modified version of the native, human CBS (hCBS) enzyme. The goal of treatment is to introduce the CBS enzyme into circulation, resulting in reduced Hcy levels, increased cystathionine (Cth) and cysteine (Cys) levels.
Study Started
Jan 22
2019
Primary Completion
Oct 31
2022
Anticipated
Study Completion
Jun 30
2025
Anticipated
Last Update
Jul 13
2022

Drug Pegtibatinase

Pegtibatinase sterile solution for subcutaneous injection

  • Other names: TVT-058, OT-58, PEG modified CBS, PEG htCBS C15S, htCBS C15S ME-200GS

Drug Placebo

Normal saline for subcutaneous injection

Pegtibatinase Active Comparator

Placebo Placebo Comparator

Criteria

Inclusion Criteria:

Confirmed diagnosis of homocystinuria based on genetic confirmation and plasma tHcy ≥50 micromoles and documentation of previous tHcy level ≥80 micromoles
Willing and able to provide written, signed informed consent and to comply with all study related procedures.
Subjects born biologically as female who are of child-bearing potential must have a negative pregnancy test at screening and be willing to have additional pregnancy tests during the study. Subjects born biologically as male who identify as female and are not of childbearing potential are not required to undergo pregnancy tests
Sexually active subjects who have childbearing potential or those who have partners of childbearing potential must be willing to use acceptable methods of contraception while on the study and for 4 weeks after the end of study
Willing to maintain a stable diet with no significant modifications while on study and complete a daily diet diary.

Exclusion Criteria:

Previous exposure to pegtibatinase and/or previous participation in a clinical trial that included administration of pegtibatinase
Use of any investigational product or investigational medical device within 30 days prior to Screening, or while on study
Use or planned use of any injectable drugs containing PEG (other than pegtibatinase or COVID-19 vaccines), including medroxyprogesterone (eg, Depo-Provera) injection, within 3 months prior to Screening and during study participation
Known hypersensitivity to PEG-containing product or any components of pegtibatinase
A positive test for HIV antibody, hepatitis B surface antigen, or hepatitis C antibody
A history of organ transplantation, chronic immunosuppressive therapy, or substance abuse
Pregnant or breastfeeding at Screening or planning to become pregnant (self or partner) or to breastfeed at any time during the study
Concurrent disease or condition or planned major surgery that would interfere with study participation or safety in the opinion of the investigator.
Any condition that, in the view of the investigator, places the subject at high risk of poor treatment compliance or of not completing the study
Major surgery planned during the study period
No Results Posted