BnH-015B Clinical Trial in Moderate Alzheimer's Disease

NCT06535308 · Status: RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 92

Last updated 2025-01-07

No results posted yet for this study

Summary

BnH-015B is a small molecule compound that targets the GluN2B binding site on NMDA receptors and positively modulates. BnH-015B has shown, through nonclinical trials, to improve symptoms of cognitive decline by regulating the BDNF/TRKβ and microglia-mediated IL-33/OPN signaling pathways; therefore, it is expected to be a promising new drug that can significantly improve symptoms associated with Alzheimer's disease, including memory loss.

Conditions

  • Alzheimer Disease

Interventions

DRUG

BnH-015B 5 mg

Korean / 3 on BnH-015B, 1 on placebo

DRUG

BnH-015B 10 mg

Korean / 6 on BnH-015B, 2 on placebo

DRUG

BnH-015B 20 mg

Korean / 6 on BnH-015B, 2 on placebo

DRUG

BnH-015B 40 mg (Dietary impact)

Korean / 6 on BnH-015B, 2 on placebo

DRUG

BnH-015B 40 mg

Caucasian / 6 on BnH-015B, 2 on placebo

DRUG

BnH-015B 80 mg

Korean / 6 on BnH-015B, 2 on placebo

DRUG

BnH-015B 160 mg

Korean / 6 on BnH-015B, 2 on placebo

DRUG

BnH-015B 40 mg (MAD)

Korean / 6 on BnH-015B, 2 on placebo

DRUG

BnH-015B 80 mg (MAD)

Korean / 6 on BnH-015B, 2 on placebo

DRUG

BnH-015B 40 mg (Part II)

Korean / 9 subjects

DRUG

BnH-015B 80 mg (Part II)

Korean / 9 subjects

DRUG

BnH-015B Placebo (Part II)

Korean / 6 subjects

Sponsors & Collaborators

  • BnH Research

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
19 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-10-22
Primary Completion
2026-04-30
Completion
2026-06-30

Countries

  • South Korea

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06535308 on ClinicalTrials.gov