TXA127 in Non-Ambulant Patients With DMD Cardiomyopathy
Study Details
Study Description
Brief Summary
This open-label, single-arm multi-center study studying the safety and efficacy of TXA127 on non-ambulant patients with DMD Cardiomyopathy will comprise of two phases:
-
6-month open-label treatment phase: Male DMD patients with documented cardiomyopathy, will receive a daily subcutaneous injection of TXA127 0.5 mg/kg. Treatment will be provided for 6 months. Treatment safety will be assessed by collection and review of AEs, vital signs, ECGs, physical examinations, PFTs, and laboratory parameters on Day 1, Month 1, and Month 6. Ejection Fraction, upper extremity strength and biomarker levels will be assessed at these study visits as well. In addition, an abbreviated safety visit will be conducted at Month 3.
-
12-month optional extension phase: Patients will continue the same study drug regime for an additional 12 months. The primary objective of this phase is to obtain long-term safety data. Efficacy data will also be collected. Safety, efficacy, and exploratory biomarkers will be assessed at Month 12 and Month 18, using the same methods as in the treatment phase. In addition, abbreviated safety visits will be conducted at Month 9 and Month 15.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
| Phase 2 |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: TXA127 SC 0.5mg/kg/day TXA127 (talfirastide) 0.5mg/kg/day given via subcutaneous injection for 6 months |
Drug: talfirastide
TXA127 (talfirastide) is a pharmaceutically formulated angiotensin (1-7) heptapeptide, identical to the endogenously produced, non-hypertensive derivative of angiotensin II (Ang II).
Other Names:
|
Outcome Measures
Primary Outcome Measures
- To evaluate the safety of TXA127 in patients with DMD [6 months plus 12 month extension]
Incidence of adverse events (AEs), their severity and relationship to treatment
- To evaluate the effects of treatment on ejection fraction (EF) [6 months plus 12 month extension]
Percent change in EF, as measured by echocardiogram (ECHO); Absolute change in EF, as measured by echocardiogram
Secondary Outcome Measures
- To evaluate the effects of treatment on upper extremity muscle function [6 months plus 12 month extension]
Percent change in upper extremity strength, as measured by grip strength with a dynamometer; Absolute change in upper extremity strength, as measured by grip strength with a dynamometer
- To evaluate the effects of treatment on fractional shortening (FS) [6 months plus 12 month extension]
Percent and absolute change in fractional shortening as measured by echocardiogram
Other Outcome Measures
- To evaluate the effects of treatment on exploratory DMD-related clinical signs, FVC [6 months plus 12 month extension]
Forced Vital Capacity (FVC) % predicted Absolute and percent (where applicable) change in the following biomarkers in the blood: Troponin and Brain Natriuretic Peptide (BNP) Brain-derived neurotrophic factor (BDNF)
- To evaluate the effects of treatment on exploratory DMD-related clinical signs, PEF [6 months plus 12 month extension]
Peak Expiratory Flow (PEF) % predicted (if available) Absolute and percent (where applicable) change in the following biomarkers in the blood: Troponin and Brain Natriuretic Peptide (BNP) Brain-derived neurotrophic factor (BDNF)
- To evaluate the effects of treatment on exploratory DMD-related biomarkers, Troponin [6 months plus 12 month extension]
Absolute and percent (where applicable) change in Troponin
- To evaluate the effects of treatment on exploratory DMD-related biomarkers, BNP [6 months plus 12 month extension]
Absolute and percent (where applicable) change in Brain Natriuretic Peptide (BNP)
- To evaluate the effects of treatment on exploratory DMD-related biomarkers, BDNF [6 months plus 12 month extension]
Absolute and percent (where applicable) change in Brain-derived neurotrophic factor (BDNF)
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Male subjects 16 years of age or older who provide informed consent and can follow up with protocol procedures. Parental or guardian consent is required for subjects at least 16 years of age but younger than 18 years of age.
-
Documented diagnosis of Duchenne muscular dystrophy by genetic mutation analysis.
-
Documented cardiomyopathy, as assessed by echocardiogram with EF >35% and <55% and fractional shortening of ≤ 28% at the time of screening.
-
Subjects must be taking systemic glucocorticoids for at least six months prior to screening.
-
Subjects taking mineralocorticoid receptor antagonists, must be taking the drug for at least three months prior to screening
-
Non-ambulant and cared for by a trained caregiver
Exclusion Criteria:
-
Therapy with intravenous inotropic or vasoactive medications at the time of screening
-
Planned or likelihood of major surgery in the 6 months after planned enrollment.
-
Patient is using a left ventricular assist device (LVAD) or actively in the process of acquiring a LVAD.
-
Estimated glomerular filtration rate (GFR) <50 mL/min, as calculated by the CKD-EPI Creatinine equation 2021 (https://www.kidney.org/professionals/kdoqi/gfr_calculator)
-
Reproducible (+/- 10%) difference between screening and baseline, percent predicted FVC between 45 and 85, inclusive, using best of 3 efforts at each visit
-
Patients with non-invasive ventilation, such as CPAP and BiPAP
-
Patient is suffering from unstable systemic allergic reaction(s), connective tissue disease or autoimmune disorder(s), requiring active intervention
-
History of cardiac tumor or current cardiac tumor
-
Known moderate-to-severe aortic stenosis/insufficiency or severe mitral stenosis/regurgitation
-
Current alcohol or drug abuse
-
Known history of chronic viral hepatitis unless considered cured based on hepatitis C RNA negative results
-
Hepatic dysfunction upon screening evidenced by bilirubin levels or gamma-GT levels above normal, deemed as clinically significant by the PI/Sub-I, and/or abnormal hematology (hematocrit <25%, WBC <3000/μl, platelets <100,000/μl), without a reversible, identifiable cause. Total bilirubin elevations > 2 times the upper reference range, consistent with Gilbert's Syndrome, may be enrolled if there is no other evidence of liver dysfunction
-
Uncontrolled diabetes (HbA1c >9.0 percent)
-
Inability to comply with protocol-related procedures, including required study visits
-
Any condition or other reason that, in the opinion of the investigator or Medical Monitor, would render the subject unsuitable for the study
-
Currently receiving or received within 90 days of enrollment (Day 1) an investigational treatment on another clinical study or expanded access protocol. This will include patients currently being treated or who have not completed follow-up to treatment with an investigational cell-based therapy within 6 months prior to enrollment and patients actively receiving an investigational therapy for cardiovascular repair/regeneration.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Hadassah Medical Center | Jerusalem | Israel | ||
| 2 | Sheba Medical Center | Ramat Gan | Israel |
Sponsors and Collaborators
- Constant Therapeutics LLC
Investigators
- Study Chair: Richard L Franklin, MD, PhD, Constant Therapeutics LLC
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- TXA127-DMD-002