Efficacy and Safety of TPN171H in the Patients With Erectile Dysfunction

PHASE2CompletedINTERVENTIONAL
Enrollment

255

Participants

Timeline

Start Date

July 23, 2020

Primary Completion Date

July 26, 2021

Study Completion Date

July 26, 2021

Conditions
Erectile Dysfunction
Interventions
DRUG

TPN171H

Pharmaceutical form;tablets Route of administration:;oral;Administered 30 minutes to 4 hours prior to initiation of sexual activity for a duration of 8 weeks to use no more than one dose in any 24-hour period

DRUG

placebo

Pharmaceutical form;tablets Route of administration:;oral;Administered 30 minutes to 4 hours prior to initiation of sexual activity for a duration of 8 weeks to use no more than one dose in any 24-hour period

Trial Locations (12)

100191

Peking University Third Hospital, Beijing

116011

The First Affiliated Hospital of Dalian Medical University, Dalian

130021

The First Hospital of Jilin University, Changchun

210008

Nanjing Drum Tower Hospital, Nanjing

215000

Second Affiliated Hospital of Suzhou University, Suzhou

230000

The First Affiliated Hospital of Anhui Medical University, Hefei

330000

The First Affiliated Hospital of Nanchang University, Nanchang

350005

The First Affiliated Hospital of Fujian Medical University, Fuzhou

410000

The Third Xiangya Hospital of Central South University, Changsha

450100

Henan Provincial People's Hospital, Zhengzhou

510000

Guangzhou First People's Hospital, Guangzhou

518036

Peking University Shenzhen Hospital, Shenzhen

All Listed Sponsors
collaborator

Shanghai Institute of Materia Medica, Chinese Academy of Sciences

OTHER

lead

Vigonvita Life Sciences

INDUSTRY

NCT04479917 - Efficacy and Safety of TPN171H in the Patients With Erectile Dysfunction | Biotech Hunter | Biotech Hunter