Ozmosi | Emraclidine Drug Profile
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Emraclidine

Alternative Names: Emraclidine, cvl-231, cvl 231, cvl231, pf-06852231, pf06852231, pf 06852231
Clinical Status: Active
Latest Update: 2025-10-21
Latest Update Note: Clinical Trial Update

Product Description

Emraclidine is an orally available muscarinic M4 Receptor (PAM) being investigated for the treatment of schizophrenia and other forms of psychosis. (Sourced from: https://www.abbvie.com/science/pipeline.html)

Mechanisms of Action: M4 PAM

Novel Mechanism: Yes

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Pfizer
Company Location: Eastern America
Company CEO: Albert Bourla
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Emraclidine

Countries in Clinic: Belgium, Bulgaria, Hungary, Puerto Rico, Ukraine, United States

Active Clinical Trial Count: 17

Recent & Upcoming Milestones

Highest Development Phases

Phase 2: Psychotic Disorders

Phase 1: Alzheimer Disease|Healthy Volunteers|Kidney Diseases|Other

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT05940402

CVL-231-SP-1007

P1

Completed

Kidney Diseases

2024-12-19

50%

2025-03-06

NCT05935033

CVL-231-SP-1008

P1

Completed

Other

2025-02-21

50%

2025-03-06

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

2024-511441-19-00

CVL-231-2003

P2

Active, not recruiting

Schizophrenia

2026-02-28

2025-05-02

Treatments

NCT05227690

CVL-231-2001

P2

Completed

Schizophrenia|Psychotic Disorders

2024-08-23

12%

2025-09-18

Primary Endpoints|Treatments

NCT05644977

CVL-231-1006

P1

Completed

Alzheimer Disease

2025-04-14

50%

2025-05-03

Primary Endpoints

NCT05933187

CVL-231-HV-1013

P1

Completed

Healthy Volunteers

2023-09-12

23%

2023-11-27

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

NCT05915546

CVL-231-HV-1009

P1

Completed

Healthy Volunteers

2023-07-26

69%

2023-11-27

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

NCT04787302

CVL-231-1002

P1

Completed

Schizophrenia

2023-07-14

48%

2023-07-28

Primary Completion Date|Primary Endpoints|Study Completion Date

NCT07145918

M25-522

P2

Recruiting

Schizophrenia

2028-02-01

12%

2025-08-29

NCT05443724

CVL-231-2003

P2

Completed

Schizophrenia

2025-06-25

12%

2025-07-29

Primary Endpoints

2022-000581-17

2022-000581-17

P2

Completed

Schizophrenia

2024-09-11

2025-05-06

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

2022-000580-52

2022-000580-52

P2

Completed

Schizophrenia

2024-08-26

12%

2025-05-06

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

NCT05227703

CVL-231-2002

P2

Completed

Schizophrenia

2024-08-15

50%

2024-12-21

NCT07219030

M25-904

P1

Recruiting

Healthy Volunteers

2026-11-01

88%

2025-10-23

NCT06366243

CVL-231-HV-1012

P1

Completed

Healthy Volunteers

2024-06-20

12%

2024-07-25

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

NCT06301971

CVL-231-HV-1011

P1

Completed

Healthy Volunteers

2024-04-04

50%

2024-05-03

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

NCT05965219

CVL-231-HV-1010

P1

Completed

Healthy Volunteers

2023-11-10

23%

2024-04-03

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