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New treatment option for Alpha-1 Antitrypsin Deficiency (AATD)
Official title A Study of TSRA-196 in Adults With PiZZ Alpha-1 Antitrypsin Deficiency (AATD)
ClinicalTrials.gov ID: NCT07227207
What this study is testing
What is TSRA-196?
TSRA-196 is an investigational medicine, given as an infusion into a vein, being studied as a potential treatment for alpha-1 antitrypsin deficiency (aatd).
Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.
- What it's testing
- This is a Phase 1/2, open-label, multi-center, dose escalation (Part 1), dose expansion (Part 2), and single repeat dose (Part 3) study to evaluate the safety, tolerability, efficacy, and PK/PD parameters of TSRA-196 in adults with the PiZZ genotype who have lung and/or liver disease associated with severe alpha-1 antitrypsin deficiency (AATD)
- Phase 2: a mid-size study of how well it works
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 70
You may be able to join if
- Males or females who are 18 to 70 years of age, inclusive, at the time of signing the informed consent
- Body mass index of 18 to 37 kg/m2, inclusive
- Confirmed diagnosis of AATD and PiZZ genotype
- At least one previous measure of blood total AAT level \<11 µmol/L
- Nonsmoker for at least 6 months before screening and must remain nonsmoking for the entire study duration
You likely can't join if
- Presence of genetic variation in SERPINA1 gene that may disrupt the function of TSRA-196, determined by screening genotyping
- History of liver disease unrelated to AATD, or history of or clinical signs of cirrhosis
- Significant lung disease not attributable to manifestations of AATD, as determined by the investigator
- History of one or more hospitalizations due to severe exacerbation of underlying lung disease during the year before screening or received IV...
- Unstable AATD-related COPD, as determined by the investigator, or severe bronchiectasis
- Lung volume reduction surgery within 1 year before screening or plan to receive lung volume reduction surgery during the study period
See the full eligibility criteria
- Males or females who are 18 to 70 years of age, inclusive, at the time of signing the informed consent
- Body mass index of 18 to 37 kg/m2, inclusive
- Confirmed diagnosis of AATD and PiZZ genotype
- At least one previous measure of blood total AAT level \<11 µmol/L
- Nonsmoker for at least 6 months before screening and must remain nonsmoking for the entire study duration
- Either AAT treatment-naïve or washed out of all investigational or approved treatments that modify AAT levels for 5 half-lives or at least 4 weeks, whichever is longer, before TSRA-196 administration Parts 1A and 2A...
- Clinically significant lung disease, defined as 1) evidence of emphysema or bronchiectasis by computed tomography or 2) DLCO \<70% of the predicted value or 3) ppFEV1 \<80%
- ppFEV1 ≥35%
- METAVIR fibrosis score F0 or F1 confirmed by liver biopsy at screening, or a liver stiffness measure by FibroScan ≤7 kPa at screening
- FIB-4 index score ≤3.25 at screening
- ALT and/or AST \<ULN at screening Parts 1B and 2B (AATD liver disease with significant or severe liver fibrosis, with or without AATD lung disease)
- METAVIR fibrosis score F2 or F3 confirmed by liver biopsy at screening. A liver biopsy conducted within 12 months before screening is acceptable as a substitute.
- Liver stiffness measure by FibroScan \>7 and ≤15 kPa at screening
- ALT and/or AST \<2 x ULN at screening
- Presence of genetic variation in SERPINA1 gene that may disrupt the function of TSRA-196, determined by screening genotyping
- History of liver disease unrelated to AATD, or history of or clinical signs of cirrhosis
- Significant lung disease not attributable to manifestations of AATD, as determined by the investigator
- History of one or more hospitalizations due to severe exacerbation of underlying lung disease during the year before screening or received IV antibiotics for treatment of a pulmonary infection within 6 months before...
- Unstable AATD-related COPD, as determined by the investigator, or severe bronchiectasis
- Lung volume reduction surgery within 1 year before screening or plan to receive lung volume reduction surgery during the study period
- Documented chronic need for positive airway pressure therapy beyond nocturnal use
- Seropositive for human immunodeficiency virus (HIV) (HIV-1 or HIV-2)
- Seropositive for hepatitis B (hepatitis B surface antigen [HBsAg] or hepatitis B core antibody [HBcAb] positive) with detectable HBV DNA
- Hepatitis C virus (HCV) RNA positive at screening (Parts 1A and 2A), or HCV RNA positive and/or HCV antibody positive at screening (Parts 1B and 2B)
- Has received an organ transplant or is on a waiting list for an organ transplant
- Prior treatment with gene therapy using viral vectors or intended to permanently change the patient's DNA
- Any investigational products within 30 days before dosing or plan to take an investigational product before the end of study
The study team makes the final eligibility decision.
Where it's taking place
- Boston, Massachusetts, United States
- Charleston, South Carolina, United States
- Seattle, Washington, United States
- Fitzroy, Victoria, Australia
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 70 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Boston, Massachusetts, United States; Charleston, South Carolina, United States; Seattle, Washington, United States; Fitzroy, Victoria, Australia. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.