Success Metrics

Clinical Success Rate
88.9%

Based on 16 completed trials

Completion Rate
89%(16/18)
Active Trials
1(5%)
Results Posted
44%(7 trials)
Terminated
2(10%)

Phase Distribution

Ph phase_4
3
15%
Ph phase_1
6
30%
Ph phase_3
10
50%

Phase Distribution

6

Early Stage

0

Mid Stage

13

Late Stage

Phase Distribution19 total trials
Phase 1Safety & dosage
6(31.6%)
Phase 3Large-scale testing
10(52.6%)
Phase 4Post-market surveillance
3(15.8%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

88.9%

16 of 18 finished

Non-Completion Rate

11.1%

2 ended early

Currently Active

1

trials recruiting

Total Trials

20

all time

Status Distribution
Active(1)
Completed(16)
Terminated(2)
Other(1)

Detailed Status

Completed16
Terminated2
unknown1
Active, not recruiting1

Development Timeline

Analytics

Development Status

Total Trials
20
Active
1
Success Rate
88.9%
Most Advanced
Phase 4

Trials by Phase

Phase 16 (31.6%)
Phase 310 (52.6%)
Phase 43 (15.8%)

Trials by Status

terminated210%
unknown15%
active_not_recruiting15%
completed1680%

Recent Activity

Clinical Trials (20)

Showing 20 of 20 trials
NCT06864793Phase 1

Study on the Pharmacokinetics and Safety of QL1012D and Gonal-F® in Healthy Female Volunteers

Active Not Recruiting
NCT06173869Phase 3

A Randomised Trial Comparing the Ovarian Response of a Starting Dose of Either 10 μg or 15 μg Follitropin Delta (FE 999049) to a Starting Dose of Either 150 IU or 225 IU Follitropin Alfa (GONAL-F) in Conventional Regimens in China

Completed
NCT02892942Phase 4

NATural Ovarian Stimulation

Completed
NCT04899193Phase 1

Pergoveris FD and Liquid China BE Study

Completed
NCT05149924Phase 3

Efficacy and Safety of QL1012 in Women for Assisted Reproductive Treatment

Completed
NCT02592031Phase 1

Study to Compare the Bioavailability, Safety and Tolerability of XM17 in Healthy, Down Regulated Young Women

Completed
NCT01297465Phase 3

PERgoveriS In Stratified Treatment for Assisted Reproductive Technique

Completed
NCT01354886Phase 1

Single Dose FSH-GEX™ in Healthy Volunteers

Completed
NCT01820728Phase 3

A Phase III Clinical Study to Compare the Efficacy and Safety of DA-3801 and That of Gonal-F®

Completed
NCT02607293

A Study to Explore Correlation Between Symptoms and Signs of Polycystic Ovarian Syndrome (PCOS) and Risk of Over-response to Ovarian Stimulation

Completed
NCT03535103Phase 1

Study on the Safety and Pharmacokinetics of LM001 and Gonal-F® in Healthy Women

Unknown
NCT01183143Phase 3

Convenience and Safety of Assisted Reproductive Technology Procedures Using a Gonal-F Filled by Mass (Fbm) Liquid Formulation Applied by Pen for Ovulation Induction and In-vitro Fertilization

Completed
NCT00249834Phase 4

Safety and Efficacy of Pre-defined, Fixed Dose of Gonal-f Pen Based on Subject Baseline Characteristics in Subjects Undergoing in Vitro Fertilization (IVF)

Completed
NCT02047227Phase 3

Phase 3 Study to Evaluate the Efficacy and Safety of Pergoveris® in Assisted Reproductive Technology (ESPART)

Completed
NCT02454556Phase 3

A Randomized, Multicentre, Open Label, Evaluator Blinded Study to Evaluate Safety and Efficacy of Folitime® of Gemabiotech S.A., Versus Gonal-f ® of Merck Serono, in Patients With Infertility Undergoing ART

Completed
NCT01871532Phase 4

Low-dose Gonal-f® in Ovulation Induction

Terminated
NCT01497197Phase 3

A Trial to Compare the Efficacy and Safety of Ovarian Stimulation With GONAL-f® and Luveris® Starting on Day 1 Versus Day 6 in Women Undergoing Assisted Reproductive Technique

Terminated
NCT00378001Phase 3

Clinical Efficacy and Tolerability of Two FSH Preparations (Human FSH Versus rFSH - Follitropin Alpha) in Women Undergoing IVF

Completed
NCT02335879Phase 3

Phase III Clinical Study of Domestic Recombinant Human Follitropin for Injection to Treat WHO Class II Anovulation

Completed
NCT01141270Phase 1

Comparative Pharmacokinetics of AFOLIA and Gonal-f® After Single Subcutaneous Application

Completed

All 20 trials loaded

Drug Details

Intervention Type
DRUG
Total Trials
20