Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 40/100

Failure Rate

12.5%

2 terminated/withdrawn out of 16 trials

Success Rate

77.8%

-8.7% vs industry average

Late-Stage Pipeline

19%

3 trials in Phase 3/4

Results Transparency

71%

5 of 7 completed trials have results

Key Signals

5 recruiting5 with results

Enrollment Performance

Analytics

Phase 2
8(61.5%)
Phase 3
3(23.1%)
Phase 1
2(15.4%)
13Total
Phase 2(8)
Phase 3(3)
Phase 1(2)

Activity Timeline

Global Presence

Loading network data...

Clinical Trials (16)

Showing 16 of 16 trials
NCT07221851Phase 3Recruiting

Trial Investigating the Efficacy and Safety of Weekly Lonapegsomatropin Compared to Daily Somatropin in Children and Adolescents With Short Stature or Growth Failure Due to Growth Hormone Sufficient Disorders

Role: lead

NCT06732895Phase 2Recruiting

A Clinical Trial to Evaluate Efficacy and Safety of Navepegritide in Adolescents (12 - 18 Years of Age) With Achondroplasia.

Role: lead

NCT07264634Recruiting

A Study to Assess the Amount of Palopegteriparatide in Breast Milk of Lactating Females Requiring YORVIPATH® (Palopegteriparatide)

Role: lead

NCT06079398Phase 2Recruiting

A Clinical Trial to Evaluate Efficacy and Safety of TransCon CNP Compared With Placebo in Infants (0 to <2 Years of Age) With Achondroplasia

Role: lead

NCT07345494Recruiting

A Global Pregnancy Registry to Assess Maternal, Fetal, and Infant Outcomes Following Exposure to YORVIPATH® (Palopegteriparatide) During Pregnancy and Breastfeeding

Role: lead

NCT05980598Phase 2Terminated

TransCon (TC) TLR7/8 Agonist, TC IL-2 β/γ, Pembrolizumab Prior to Surgery for Advanced Head and Neck Squamous Cell Carcinoma

Role: lead

NCT04085523Phase 2Completed

A Dose Escalation Trial Evaluating Safety, Efficacy, and Pharmacokinetics of TransCon CNP Administered Once Weekly in Prepubertal Children With Achondroplasia

Role: lead

NCT04009291Phase 2Completed

A Trial Investigating the Safety, Tolerability and Efficacy of TransCon PTH in Adults With Hypoparathyroidism

Role: lead

NCT03344458Phase 3Completed

A Long-Term Trial Investigating Safety and Efficacy of TransCon hGH in Children With Growth Hormone Deficiency Who Have Completed a Prior TransCon hGH Clinical Trial

Role: lead

NCT03875534Completed

A Multi-center, Longitudinal, Observational Study of Children With Achondroplasia

Role: lead

NCT05246033Phase 2Unknown

A Dose Escalation Trial Evaluating Safety, Efficacy, and Pharmacokinetics of Multiple Subcutaneous Doses of TransCon CNP Administered Once Weekly in Children With Achondroplasia

Role: lead

NCT04326374Phase 3Unknown

Safety, Tolerability and Efficacy of TransCon hGH Weekly Versus Daily hGH in Chinese Pediatric Growth Hormone Deficiency

Role: collaborator

NCT03803163Phase 1Terminated

A Safety, Tolerability and Pharmacokinetics Study of TransCon Treprostinil in Healthy Adult Male Volunteers

Role: lead

NCT01247675Phase 2Completed

A Safety, Pharmacokinetic and Pharmacodynamic Study of ACP-001 (TransCon hGH) in Adults With Growth Hormone Deficiency

Role: lead

NCT01947907Phase 2Completed

Safety, PK/PD (Pharmacokinetics/Pharmacodynamics) and Efficacy of ACP-001 Weekly Versus Daily hGH in Children With Growth Hormone Deficiency (GHD)

Role: lead

NCT01010425Phase 1Completed

Pharmacokinetics and Pharmacodynamics of ACP-001 (TransCon PEG hGH)

Role: lead

All 16 trials loaded