Veri-T: A Trial of Verdiperstat in Patients With svPPA Due to TDP-43 Pathology

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

PHASE1

Total Enrollment

64 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-04-14

Study Completion Date

2026-09-30

Brief Summary

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The purpose of the study is to test the safety and tolerability of twice daily Verdiperstat in patients with semantic variant primary progressive aphasia (svPPA) due to frontotemporal lobar degeneration with TDP-43 pathology (FTLD-TDP). Three-fourths of the participants will receive Verdiperstat and one-fourth will receive Placebo during the 24-week treatment duration.

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Detailed Description

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This is a Phase 1, randomized, double-blind, placebo-controlled study of the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary efficacy of Verdiperstat in patients with semantic variant primary progressive aphasia (svPPA) due to frontotemporal lobar degeneration with TDP-43 pathology (FTLD-TDP). Approximately 64 subjects will be randomized 3:1 to active drug or placebo. Study drug will be administered orally bid (two Verdiperstat tablets bid or two placebo tablets bid (for a total daily dose of 600mg daily, following a one-week titration period of 1 tablet daily).

The study will test the effects of Verdiperstat on cerebrospinal fluid (CSF) proteins, brain magnetic resonance imaging (MRI), and cognitive (thinking, memory and language) tests in subjects with svPPA due to FTLD-TDP. This study uses placebo which looks like the experimental drug but does not have any active drug in it.

Conditions

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Semantic Dementia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Randomized, Double-Blind, Placebo-Controlled

Primary Study Purpose

TREATMENT

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Double-blind study. Only investigational pharmacist will be unblinded

Study Groups

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Verdiperstat

Verdiperstat 2 tablets twice daily (600mg total daily) by mouth for 24 weeks.

Group Type EXPERIMENTAL

Verdiperstat

Intervention Type DRUG

Oral, extended release (ER) tablet

Placebo

Placebo 2 tablets twice daily by mouth for 24 weeks.

Group Type PLACEBO_COMPARATOR

Verdiperstat

Intervention Type DRUG

Oral, extended release (ER) tablet

Interventions

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Verdiperstat

Oral, extended release (ER) tablet

Intervention Type DRUG

Other Intervention Names

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BHV-3241

Eligibility Criteria

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Inclusion Criteria

1. Between 18 and 85 years of age (inclusive) at the initial screening visit;
2. Meets 2011 consensus criteria for svPPA (Gorno-Tempini et al. 2011);
3. MRI at screening is consistent with the underlying svPPA with no large strokes or severe white matter disease (Fazekas Grade ≤2; Fazekas et al. 1987);
4. CDR® plus NACC FTLD (Miyagawa et al. 2020) global score at screening ≤1;
5. The following medications are allowed, but must be stable for 2 months prior to the initial screening visit:

1. Food and Drug Administration (FDA)-approved Alzheimer's disease (AD) medications;
2. FDA-approved psychotropic medications;

Exclusion Criteria

7. Has a reliable study partner who agrees to accompany the participant to visits, and spends at least 5 hours per week with the participant;
8. Agrees to 2 LPs;
9. Signed and dated written informed consent obtained from the participant and the participant's study partner in accordance with local Institutional Review Board (IRB) regulations;
10. WOCBP must agree to abstain from sex or use highly effective birth control that includes two methods of contraception (one of which must be a barrier method) for the duration of the screening period, the RDBPC treatment period, and for 30 days after the last dose of study drug (active or placebo);
11. Males must agree to abstain from sex with WOCBP or use an adequate method of contraception for the duration of the RDBPC treatment period and for 90 days after the last dose of study drug (active or placebo);
12. Able to swallow pills whole without crushing or chewing.

1. A clinical diagnosis of probable AD (McKhann et al. 2011) or previous biomarker evidence of AD biology using amyloid positron emission tomography (PET) imaging, CSF amyloid beta (Aβ)/total tau (t-tau) ratio, CSF/plasma amyloid beta isoform with 40 amino acid residues (Aβ40)/amyloid beta isoform with 42 amino acid residues (Aβ42) ratio, or plasma phosphorylated tau \[phosphorylated tau at residue 181 (p-tau181) and phosphorylated tau at residue 217 (p-tau217)\] assessments;
2. A clinical diagnosis of a comorbid FTLD-associated clinical syndrome other than svPPA, including:

1. logopenic primary progressive aphasia (lvPPA; Gorno-Tempini et al. 2011);
2. non-fluent/agrammatic variant primary progressive aphasia (nfvPPA; Gorno-Tempini et al. 2011);

* c. behavioral variant for frontotemporal dementia (bvFTD; Rascovsky et al. 2011). Patients who meet diagnostic criteria for svPPA (Gorno-Tempini et al. 2011) may still be included if they have a secondary diagnosis of bvFTD, so long as the PI can reasonably attribute their disinhibition, dietary changes, compulsions, and/or loss of empathy to anterior temporal lobe atrophy (Seeley et al. 2005) and MRI is consistent with right anterior atrophy (or left temporal atrophy in participants with suspected right hemispheric language dominance);

d. progressive supranuclear palsy (PSP; Höglinger et al. 2017); e. corticobasal syndrome (CBS; Armstrong et al. 2013);
3. Any other medical condition other than FTLD that is likely to account for cognitive or behavioral deficits (e.g., uncontrolled seizure disorder, stroke, vascular dementia, substance abuse or alcoholism, Lewy body disease);
4. History of uncontrolled thyroid disease or evidence thereof \[i.e., abnormal free thyroxine (T4) levels and thyroid stimulating hormone (TSH) \> 10 milli-international units (mIU)/liter (L) at screening (confirmed by repeat)\];
5. Serious autoimmune disease, or ongoing immunocompromised state;
6. History of significant cardiovascular, hematologic, renal, or hepatic disease (or laboratory evidence thereof at screening);
7. History or presence of gastrointestinal (GI) or other disease known to interfere with absorption, distribution, metabolism, or excretion of drugs, or a history of surgery known to interfere with absorption or excretion of drugs (i.e., gastric bypass);
8. Within 1 year prior to initial screening visit or between screening and baseline (pre-dose Day 1), any of the following: myocardial infarction; hospitalization for congestive heart failure; hospitalization for, or symptoms of, unstable angina; or syncope;
9. History of major psychiatric illness or untreated depression that in the opinion of the PI would pose a safety risk or interfere with the appropriate interpretation of study data;
10. Neutrophil count \<1,500/cubic millimeter (mm3), platelets \<100,000/mm3, serum creatinine \>1.5 x upper limit of normal (ULN), total bilirubin (TBL) \>1.5 x ULN, alanine aminotransferase (ALT) \>1.5 x ULN, aspartate aminotransferase (AST) \>1.5 x ULN, or international normalized ratio (INR) \>1.2 at screening (confirmed by repeat);
11. Evidence of any clinically significant findings on screening or baseline evaluations which, in the opinion of the PI would pose a safety risk or interfere with appropriate interpretation of study data;
12. Corrected QT interval by Fridericia (QTcF) ≥ 470 milliseconds (msec) or uncontrolled arrhythmia or frequent premature ventricular contractions (PVCs; \>5/minute) or Mobitz Type II second or third degree atrioventricular (AV) block or left bundle branch block or right bundle branch block with a QRS duration ≥ 150 msec or intraventricular conduction defect with a QRS duration ≥ 150 msec or evidence of acute or sub-acute myocardial infarction or ischemia or other ECG findings at screening or baseline that, in the PI's opinion, would preclude participation in the study;
13. Pathologic renal findings at screening as defined by the presence of either of the following criteria:

1. Estimated glomerular filtration rate (eGFR) \[determined by the Modification of Diet in Renal Disease (MDRD) Study equation\] \< 30 milliliter (mL)/minute/1.73 square meter (m2). The MDRD Study equation is as follows: eGFR (mL/minute/1.73 m2) = 175 x (Scr)-1.154 x (Age)-0.203 x (0.742 if female) x (1.212 if African American), where Scr = serum creatinine in mg/deciliter (dL) as measured by a method calibrated to an isotope dilution mass spectrometry (IDMS) reference method;
2. Serum creatinine ≥ 2.5 mg/dL;
14. Hemoglobin A1C \>7.5% at screening (confirmed by repeat);
15. Current or recent history (within four weeks prior to initial screening visit) of a clinically significant bacterial, fungal, or mycobacterial infection;
16. Current clinically significant viral infection, including "known" positive status for human immunodeficiency virus (HIV) (i.e., based on prior testing; HIV testing will not be performed as part of the screening evaluations for this trial);
17. Major surgery within four weeks prior to initial screening visit;
18. Blood transfusion within 4 weeks of initial screening visit;
19. History of stem cell treatment;
20. Any contraindication for MRI or unable to tolerate MRI at screening;
21. Any contraindication to or unable to tolerate LP at screening, including the use of anti-coagulant medications such as warfarin. Daily administration of 81 mg aspirin will be allowed as long as the dose is stable for 30 days prior to the initial screening visit;
22. Participants who, in the opinion of the PI, are unable or unlikely to comply with the dosing schedule or study evaluations;
23. Prior treatment with verdiperstat;
24. Treatment with another investigational drug within 30 days or 5 half-lives of drug before initial screening visit, whichever is longer. Treatment with investigational drugs other than verdiperstat while on study will not be allowed;
25. Treatment with systemic corticosteroids or steroid sparing systemic immunosuppressive agents within 30 days or 5 half-lives of drug before initial screening visit, whichever is longer. Treatment with systemic corticosteroids or other systemic immunosuppressive therapy while on study will not be allowed;
26. Treatment with strong inhibitors of CYP1A2 (i.e., ciprofloxacin, enoxacin, fluvoxamine) within 30 days or 5 half-lives of drug before initial screening visit, whichever is longer. Treatment with strong inhibitors of CYP1A2 while on study will not be allowed;
27. Known hypersensitivity to the inactive ingredients in the study drug products (active or placebo);
28. Known to be pregnant or lactating, or positive pregnancy test at screening or baseline (pre-dose Day 1);
29. Cancer within 5 years of initial screening visit, except for basal cell carcinoma;
30. History or evidence at screening of known disease-associated mutations associated with FTLD without trans-activation response deoxyribonucleic acid-binding protein of 43 kilodaltons (TDP-43) inclusions \[e.g., mutations in the genes encoding chromatin-modifying protein/charged multivesicular body protein B2 (CHMPB2), microtubule-associated protein tau (MAPT), or fused in sarcoma (FUS)\].

Minimum Eligible Age

18 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No