Key Insights

Highlights

Success Rate

87% trial completion (above average)

Published Results

23 trials with published results (64%)

Clinical Risk Assessment

Based on trial outcomes

Low Risk

Score: 15/100

Termination Rate

11.1%

4 terminated out of 36 trials

Success Rate

86.7%

+0.2% vs benchmark

Late-Stage Pipeline

58%

21 trials in Phase 3/4

Results Transparency

88%

23 of 26 completed with results

Key Signals

23 with results87% success

Data Visualizations

Phase Distribution

34Total
Not Applicable (5)
P 1 (1)
P 2 (7)
P 3 (16)
P 4 (5)

Trial Status

Completed26
Terminated4
Unknown3
Not Yet Recruiting2
Withdrawn1

Trial Success Rate

86.7%

Benchmark: 86.5%

Based on 26 completed trials

Clinical Trials (36)

Showing 20 of 20 trials
NCT07431957Phase 4Not Yet RecruitingPrimary

"Efficacy and Safety of Linaclotide in Chronic Constipation"

NCT06736912Phase 1Not Yet RecruitingPrimary

This Study Aims to Evaluate the Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Properties and Food Effect of IN-114199 in Healthy Participants

NCT03879239Not ApplicableCompletedPrimary

Efficacy and Safety of Vibrant Capsule vs. Placebo for the Treatment of Chronic Idiopathic Constipation

NCT04458675Phase 4CompletedPrimary

Efficacy and Safety of Vibrant Capsule vs. Vibrant Placebo for the Treatment of Chronic Idiopathic Constipation (CIC)

NCT04804267Phase 3UnknownPrimary

Evaluation of Clinical Equivalence Between Two Linaclotide Products in the Treatment of Chronic Idiopathic Constipation

NCT02481947Phase 3CompletedPrimary

A Safety and Efficacy Evaluation of BLI400 Laxative in Constipated Adults

NCT02819297Phase 3Completed

BLI400-302: A Safety and Efficacy Evaluation of BLI400 Laxative in Constipated Adults

NCT02819310Phase 3Completed

An Open Label Study of Chronic Use of BLI400 Laxative in Constipated Adults

NCT03097861Phase 3CompletedPrimary

Evaluation of the Bioequivalence of Sprinkle and Capsule Formulations of Lubiprostone, as Compared to Placebo

NCT01053962Phase 2CompletedPrimary

SP-304 Dose Ranging Study in Patients With Chronic Idiopathic Constipation

NCT01982240Phase 3CompletedPrimary

12-Week Study of Plecanatide for CIC (The CIC3 Study)

NCT01993875Phase 3CompletedPrimary

Pharmacodynamic, Pharmacokinetic, and Tolerability Study of a Liquid Form of Lubiprostone in Adult Subjects With Chronic Idiopathic Constipation

NCT03551873CompletedPrimary

A Postmarketing Study of Plecanatide in Breast Milk of Lactating Women Treated With TRULANCE®

NCT03120520Phase 2CompletedPrimary

An Efficacy and Safety Study of Plecanatide in Adolescents 12 to <18 Years of Age With Chronic Idiopathic Constipation

NCT02590432Phase 4Completed

An Open-Label, Long-term Study to Assess the Immunogenicity of LINZESS® (Linaclotide) Administered Orally to Adult Participants With Irritable Bowel Syndrome With Constipation or Chronic Idiopathic Constipation

NCT03054506Not ApplicableCompleted

The Effect of CSP01 on Chronic Idiopathic Constipation and Irritable Bowel Syndrome With Constipation

NCT01919697Phase 3CompletedPrimary

Open-label Extension (OLE) Study of Plecanatide for Chronic Idiopathic Constipation (CIC)

NCT02239510Not ApplicableTerminatedPrimary

Efficacy of Linaclotide to Senna for CIC

NCT02122471Phase 3CompletedPrimary

12-Week Study of Plecanatide for CIC (The National CIC3 Study)

NCT01429987Phase 2CompletedPrimary

The Plecanatide Chronic Idiopathic Constipation (CIC) Study

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