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Serlopitant

Alternative Names: serlopitant, vpd-737, mk-0594, mk0594, mk 0594
Clinical Status: Inactive
Latest Update: 2022-12-23
Latest Update Note: Clinical Trial Update

Product Description

Serlopitant, an oral, once-daily neurokinin 1 receptor antagonist, for treatment of psoriatic pruritus in a phase 2, randomized clinical trial (NCT03343639).

Mechanisms of Action: NK1 Antagonist

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Vyne Therapeutics
Company Location: BRIDGEWATER NJ 08807
Company CEO: David Domzalski
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 3: Pruritus|Neurodermatitis|Prurigo|Psoriasis|Dermatitis, Atopic

Phase 2: Urinary Incontinence|Alcoholism|Overactive Bladder|Pruritus|Psoriasis|Burns Unspecified|Refractory Chronic Cough|Prurigo|Epidermolysis Bullosa|Neurodermatitis|Dermatitis, Atopic|Unexplained Chronic Cough

Phase 1: Kidney Diseases

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

JapicCTI-173742

P1

Completed

Kidney Diseases

None

NCT03836001

P2

Completed

Pruritus|Epidermolysis Bullosa

2021-12-06

2022-12-24

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

MTI-117

P2

Completed

Pruritus

2019-12-10

55%

2021-05-20

Primary Endpoints

MTI-109

P2

Completed

Psoriasis|Pruritus

2018-10-23

62%

2021-05-20

Primary Endpoints|Treatments

2017-003250-16

P2

Completed

Unexplained Chronic Cough|Refractory Chronic Cough

2018-09-06

20%

2022-03-13

Treatments

MTI-110

P2

Completed

Unexplained Chronic Cough|Refractory Chronic Cough

2018-08-15

20%

2021-05-20

Primary Endpoints|Treatments

NCT02654483

P2

Completed

Epidermolysis Bullosa|Pruritus

2018-06-28

34%

2021-05-20

Primary Endpoints

ATOMIK

P2

Completed

Pruritus|Dermatitis, Atopic

2018-01-16

60%

2021-05-20

Primary Endpoints|Treatments

AUBURN

P2

Terminated

Burns Unspecified|Pruritus

2017-01-17

2021-05-20

Primary Endpoints|Treatments

Study of the Neurokinin-1 Receptor Antagonist VPD-737 in Subjects with Prurigo Nodularis

P2

Completed

Pruritus

2016-06-08

2022-03-13

Treatments

TCP-102

P2

Completed

Prurigo|Neurodermatitis

2016-05-27

2021-05-20

Primary Endpoints|Treatments

Study of the Neurokinin-1 Receptor Antagonist VDP-737 in Subjects with Chronic Pruritus

P2

Completed

Pruritus

2014-12-02

2022-03-13

Treatments

TCP 101

P2

Completed

Pruritus

2014-12-02

2022-05-14

Primary Completion Date|Primary Endpoints|Study Completion Date|Treatments

2008-004686-26

P2

Completed

Alcoholism

2010-03-11

2022-03-12

Treatments

MK0594-020

P2

Terminated

Alcoholism

2010-03-11

2021-05-20

Primary Endpoints|Treatments

MK-0594 Overactive Bladder Dose-Ranging Study

P2

Terminated

Overactive Bladder

2007-09-24

2022-03-12

Treatments

ND

P2

Terminated

Overactive Bladder

2007-09-24

2022-03-12

Treatments

MK0594-003

P2

Completed

Overactive Bladder|Urinary Incontinence

2007-08-01

2021-05-20

Primary Endpoints|Treatments

JapicCTI-173781

P2

Terminated

Pruritus

None

Itch

P3

Terminated

Pruritus|Prurigo|Psoriasis|Dermatitis, Atopic

2020-04-08

16%

2021-05-20

Primary Endpoints|Treatments

2017-004210-25

P3

Completed

Pruritus|Prurigo

2020-02-06

8%

2022-03-13

Treatments

MTI-105

P3

Completed

Neurodermatitis|Pruritus|Prurigo

2020-01-14

15%

2021-05-20

Primary Endpoints|Treatments

MTI-106

P3

Completed

Pruritus|Neurodermatitis|Prurigo

2020-01-09

8%

2021-05-20

Primary Endpoints

2017-004211-40

P3

Terminated

Pruritus|Dermatitis, Atopic|Psoriasis|Prurigo

2019-08-07

16%

2022-03-13

Treatments