Ozmosi | NIO-752 Drug Profile
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NIO-752

Alternative Names: NIO-752, NIO 752, NIO752
Clinical Status: Active
Latest Update: 2025-08-28
Latest Update Note: Clinical Trial Update

Product Description

NIO-752 is a drug candidate from Novartis Pharmaceutical for use in patients with progressive supranuclear palsy (PSP). (Sourced from: https://clinicaltrials.gov/ct2/show/NCT04539041)

Mechanisms of Action: Tau Antagonist

Novel Mechanism: Yes

Modality: Antibody Drug Conjugate

Route of Administration: Injection

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Novartis
Company Location: Europe
Company CEO: Vasant Narasimhan
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for NIO-752

Countries in Clinic: Canada, Finland, France, Germany, Spain, Sweden, United Kingdom, United States

Active Clinical Trial Count: 3

Recent & Upcoming Milestones

Highest Development Phases

Phase 1: Alzheimer Disease|Arthrogryposis|Brain Diseases|Cognitive Dysfunction|Memory Disorders|Paralysis|Progressive Supranuclear Palsy|Supranuclear Palsy, Progressive|Tauopathies

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT05469360

CNIO752B12201

P1

Recruiting

Alzheimer Disease|Tauopathies|Memory Disorders|Brain Diseases|Cognitive Dysfunction

2026-09-11

50%

2025-08-29

Patient Enrollment|Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments|Trial Status

NCT06372821

NIO-SILK

P1

Recruiting

Alzheimer Disease|Arthrogryposis

2026-07-01

2025-07-31

Primary Completion Date|Primary Endpoints|Start Date|Study Completion Date|Treatments|Trial Status

NCT04539041

CNIO752A02101

P1

Completed

Paralysis|Supranuclear Palsy, Progressive|Progressive Supranuclear Palsy

2024-10-17

4%

2024-11-21

Primary Endpoints|Treatments|Trial Status