Approval Probability
TA Base Rate
Adjusted LOA
ML Risk
Plecanatide · 11 trials · 5 indications
Number of participants with adverse events with evidence to suggest a causal relationship between treatment and study drug.
An Overall Responder was a patient who was a weekly responder (i.e., decrease of 30% from baseline for abdominal pain intensity and an increase of at least 1 complete spontaneous bowel movement in the same week) for at least 6 of the 12 treatment weeks.
An Abdominal Pain Intensity Responder was a patient who had a decrease of 30 % from baseline for abdominal pain intensity. Baseline is the mean of non-missing abdominal pain scores recorded during the 2-week baseline diary assessment period prior to the first dose of study drug.
A Stool Frequency Responder was a patient who experienced an increase of at least one CSBM (complete spontaneous bowel movement) per week from baseline. Baseline was the mean number of CSBMs recorded during the 2-week baseline diary assessment period prior to the first dose of study drug.
The primary efficacy endpoint was measured by the number of durable overall CSBM responders over the 12-week Treatment Period. A durable overall CSBM responder was defined as a weekly CSBM responder for at least 9 of the 12 treatment weeks, including at least 3 of the last 4 weeks. A CSBM weekly responder was defined as a patient who has ≥ 3 Complete Spontaneous Bowel Movements (CSBMs) per week and an increase from baseline of ≥1 CSBM for that week. A CSBM was a bowel movement that occurred in the absence of laxative use within 24 hours and was associated with the feeling of complete evacuation.
A durable overall CSBM responder was defined as a weekly CSBM responder for at least 9 of the 12 treatment weeks, included at least 3 of the last 4 weeks. A CSBM weekly responder was defined as a patient who has ≥ 3 Complete Spontaneous Bowel Movements (CSBMs) per week and an increase from baseline of ≥1 CSBM for that week. A CSBM was a bowel movement that occurred in the absence of laxative use within 24 hours and was associated with the feeling of complete evacuation.
All clinically significant findings upon Physical Examinations of the Safety Population during the treatment period were reported as TEAEs. Safety was evaluated based on number of patients who experienced at least one TEAE.
Tolerability was evaluated based on number of patients who experienced at least one TEAE leading to discontinuation of the study drug
The vital signs included in the assessments were blood pressure (systolic and diastolic; mmHg), heart rate (beats per minute), body temperature (°C) and respiration rate (breaths per minute).
The vital signs included in the assessments were blood pressure (systolic and diastolic; mmHg), heart rate (beats per minute), body temperature (°C) and respiration rate (breaths per minute).
The vital signs included in the assessments were blood pressure (systolic and diastolic; mmHg), heart rate (beats per minute), body temperature (°C) and respiration rate (breaths per minute).
The vital signs included in the assessments were blood pressure (systolic and diastolic; mmHg), heart rate (beats per minute), body temperature (°C) and respiration rate (breaths per minute).
Baseline was defined as the last non-missing value collected prior to first dose of study drug)
Baseline was defined as the last non-missing value collected prior to first dose of study drug within a given entry into the study. The Common Terminology Criteria for Adverse Events (CTCAE), Grades 1 through 5 were used for descriptions of severity for each Adverse Event (AE): Grade 1 - Mild; asymptomatic or mild symptoms; clinical or diagnostic observations only; intervention not indicated; Grade 2 - Moderate; minimal, local or noninvasive intervention indicated; limiting age appropriate instrumental Activities of Daily Living (ADL); Grade 3 - Severe or medically significant but not immediately life-threatening; hospitalization or prolongation of hospitalization indicated; disabling; limiting self care ADL; Grade 4 - Life-threatening consequences; urgent intervention indicated; Grade 5 - Death related to AE.
Spontaneous bowel movements (SBMs) are defined as bowel movements that occur without the use of rescue medication within the preceding 24 hours. Weekly SBM frequency will be calculated based on daily electronic diary entries. The endpoint is the change from baseline in the number of SBMs per week at Week 8.
Weekly SBM rate computed for each week
An Overall Responder is a participant who was a Spontaneous Bowel Movement (SBM) responder for the last 2 weeks of the Treatment Period. An SBM responder is defined as a participant who had \>3 SBMs per week. SBM was defined as a bowel movement that occurs in the absence of laxative use within the preceding 24 hours. Participants missing with respect to the outcome measure were scored as non-responders.
The primary efficacy endpoint was the change from baseline in the weekly CSBM frequency (CSBMs per week minus CSBMs per week at baseline) over a 12-week Treatment Period. A Complete Spontaneous Bowel Movement (CSBM) is a Bowel Movement (BM) that occurs in the absence of laxative use within 24 hours of the BM and the patient reports a feeling of complete evacuation.
A Complete Spontaneous Bowel Movement (CSBM) is a Bowel Movement (BM) that occurs in the absence of laxative use within 24 hours of the BM and the patient reports a feeling of complete evacuation. A weekly responder will have 3 or more CSBMs and an increase of at least one CSBM from baseline in the same week. An overall responder is a patient who is a weekly responder for at least 9 of the 12 treatment weeks, including at least 3 of the last 4 weeks.
| Arm | Type | Description |
|---|---|---|
| Plecanatide | EXPERIMENTAL | Plecanatide 6.0 mg tablets |
| 3.0 mg plecanatide | ACTIVE_COMPARATOR | Plecanatide 3.0 mg dosed daily for 12 weeks |
| 6.0 mg plecanatide | ACTIVE_COMPARATOR | Plecanatide 6.0 mg dosed daily for 12 weeks |
| Matching placebo | ACTIVE_COMPARATOR | Placebo dosed daily for 12 weeks |
| Plecanatide 3.0 mg | EXPERIMENTAL | Plecanatide tablets 3.0 mg QD for 12 weeks |
| Placebo | PLACEBO_COMPARATOR | Matching placebo tablets QD for 12 weeks |
| Plecanatide 6.0 mg | EXPERIMENTAL | Plecanatide tablets 6.0 mg QD for 12 weeks |
| Bisacodyl | OTHER | Rescue medication |
| Low Dose Plecanatide | EXPERIMENTAL | Participants will receive weight-based low-dose plecanatide administered orally once daily for 8 weeks. |
| High Dose Plecanatide | EXPERIMENTAL | Participants will receive weight-based high-dose plecanatide orally once daily for 8 weeks. |
| 0.5 mg plecanatide | EXPERIMENTAL | Plecanatide 0.5 mg Taken orally once daily for 4 weeks Group A: 6 to 11 years old |
| 1.0 mg plecanatide - Group A | EXPERIMENTAL | Plecanatide 1.0 mg Taken orally daily for 4 weeks Group A: 6 to 11 years old |
| 2.0 mg plecanatide | EXPERIMENTAL | Plecanatide 2.0 mg Taken orally daily for 4 weeks Group B: 12 to 18 Years of Age |
| Matching placebo - Group A | PLACEBO_COMPARATOR | Matching placebo Taken orally daily for 4 weeks Group A: 6 to 11 years old |
| 1.0 mg plecanatide - Group B | EXPERIMENTAL | Plecanatide 1.0 mg Taken orally daily for 4 weeks Group B: ≥ 12 to \< 18 Years of Age |
| Matching Placebo - Group B | PLACEBO_COMPARATOR | Matching placebo Taken orally daily for 4 weeks Group B: 12 to \< 18 years old |
| Plecanatide 0.5 mg | EXPERIMENTAL | Taken orally once daily in the morning for 8 weeks |
| Plecanatide 1.0 mg | EXPERIMENTAL | Taken orally once daily in the morning for 8 weeks |
| Plecanatide 1.5 mg | EXPERIMENTAL | Taken orally once daily in the morning for 8 weeks |
| Plecanatide 0.3mg | ACTIVE_COMPARATOR | Plecanatide 0.3mg, one tablet by mouth daily for 12 weeks |
| Plecanatide 1.0mg | ACTIVE_COMPARATOR | Plecanatide 1.0mg one tablet by mouth daily for 12 weeks |
| Plecanatide 3.0mg | ACTIVE_COMPARATOR | Plecanatide 3.0mg, one tablet by mouth daily for 12 weeks |
| Plecanatide 9.0mg | ACTIVE_COMPARATOR | Plecanatide 9.0mg, one tablet by mouth daily for 12 weeks |
| plecanatide 0.3 mg | EXPERIMENTAL | Subjects receive plecanatide 0.3 mg for 12 consecutive weeks |
| Name | Type | Description |
|---|---|---|
| Plecanatide | DRUG | - |
| Placebo | DRUG | - |
| Bisacodyl | DRUG | Rescue medication |
| Matching placebo | DRUG | Taken orally daily for 4 weeks |
Inclusion Criteria: Patients with documented diagnosis of IBS-C who: * Completed plecanatide study SP304203-04 or SP304203-05, were compliant with the previous study's requirements, and did not experience any Serious Adverse Event (SAE) deemed related to study drug during the course of the previou...
Plecanatide is an investigational small molecule being studied for gastrointestinal conditions including chronic idiopathic constipation, irritable bowel syndrome, irritable bowel syndrome with constipation, and functional constipation. It is being evaluated in clinical trials for these indications, with a focus on patients with constipation-predominant forms of irritable bowel syndrome.
Plecanatide is a peptide-based small molecule, belonging to the -tide class of drugs. Its mechanism of action involves targeting the gastrointestinal system to address constipation-related conditions. The drug is designed to act locally in the gut to help regulate bowel function in conditions like irritable bowel syndrome with constipation.
Plecanatide is being developed by Bausch Health Companies Inc., a company publicly traded under the ticker symbol BHC. The company is conducting clinical trials to evaluate the drug's safety and efficacy for treating gastrointestinal conditions such as irritable bowel syndrome with constipation and functional constipation.
Plecanatide is currently in Phase 3 clinical development. It has completed multiple Phase 3 trials for irritable bowel syndrome with constipation, and there is an active Phase 2 trial in pediatric patients with functional constipation. The drug is investigational and has not been approved by regulatory authorities.
Plecanatide has been studied in several clinical trials, including NCT01722318, a Phase 2 study in irritable bowel syndrome with constipation, and NCT02387359 and NCT02493452, both Phase 3 studies in the same condition. An active trial, NCT07723924, is evaluating the drug in children aged 6 to 18 with functional constipation.
Plecanatide is a distinct investigational drug being developed by Bausch Health. It belongs to the -tide class of peptides and is being studied specifically for constipation-predominant conditions. No alternative names for Plecanatide have been established in the clinical trial data, and it is not marketed under any other name.