Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Low Risk

Score: 15/100

Failure Rate

5.3%

1 terminated/withdrawn out of 19 trials

Success Rate

94.7%

+8.2% vs industry average

Late-Stage Pipeline

37%

7 trials in Phase 3/4

Results Transparency

56%

10 of 18 completed trials have results

Key Signals

10 with results

Enrollment Performance

Analytics

Phase 1
10(52.6%)
Phase 3
7(36.8%)
Phase 2
2(10.5%)
19Total
Phase 1(10)
Phase 3(7)
Phase 2(2)

Activity Timeline

Global Presence

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Clinical Trials (19)

Showing 19 of 19 trials
NCT05299554Phase 3Completed

Long-term Safety Study of Chronocort in the Treatment of Participants With Congenital Adrenal Hyperplasia

Role: lead

NCT05063994Phase 3Completed

Comparison of Chronocort Versus Standard Hydrocortisone Replacement Therapy in Participants Aged 16 Years and Over With Congenital Adrenal Hyperplasia

Role: lead

NCT03062280Phase 3Completed

A Study of the Efficacy, Safety and Tolerability of Chronocort in Treating CAH

Role: lead

NCT05222152Phase 2Completed

Chronocort Versus Plenadren Replacement Therapy in Adults With Adrenal Insufficiency

Role: lead

NCT02408068Phase 1Completed

Effect of Slow Release Hydrocortisone on Fed & Fasting Volunteers; Immediate Release on Fasting Only

Role: lead

NCT02720952Phase 3Completed

Treatment of Adrenal Insufficiency in Children

Role: lead

NCT01960530Phase 1Completed

An Investigational Study of Hydrocortisone

Role: lead

NCT00519818Phase 1Completed

Comparison of Two Forms of Hydrocortisone in Patients With Congenital Adrenal Hyperplasia

Role: lead

NCT03532022Phase 3Withdrawn

Open-label Comparison of Chronocort® Versus Standard Glucocorticoid Replacement Therapy

Role: lead

NCT02716818Phase 3Completed

Comparison of Chronocort® With Standard Glucocorticoid Therapy in Patients With Congenital Adrenal Hyperplasia

Role: lead

NCT03343327Phase 1Completed

A Study of Chronocort® Versus Cortef ® in Healthy Adult Male Subjects

Role: lead

NCT02966652Phase 1Completed

Study to Compare DITEST to Testosterone Undecanoate in Adult Men With Hypogonadism

Role: lead

NCT02733367Phase 3Completed

Extension Study for Patients Entered Into Study Infacort 003

Role: lead

NCT03311932Phase 1Completed

A Study of Infacort® Versus Cortef® in Healthy Adult Male and Female Subjects

Role: lead

NCT02777268Phase 1Completed

Comparison of Pharmacokinetics of Infacort® Versus Immediate-release Hydrocortisone

Role: lead

NCT03178214Phase 1Completed

Bioavailability of Infacort When Administered Onto Food Compared to Direct Oral Administration

Role: lead

NCT01735617Phase 2Completed

Pilot Study to Characterize and Examine the Pharmacokinetics and Efficacy of Chronocort® in Adults With CAH

Role: lead

NCT03051893Phase 1Completed

A Two-part, Study to Compare the Pharmacokinetics and Dose Proportionality of up to 6 Chronocort Formulations

Role: lead

NCT03019614Phase 1Completed

An Open Label Study in Healthy Volunteers to Compare Chronocort® to Hydrocortisone

Role: lead

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