plecanatide
Trade name: trulance
Approved
Jan 19, 2017
Plecanatide (SP-304) is a synthetic, 16-amino acid peptide with 2 disulfide bonds that is a secondin-class guanylate cyclase-C (GC-C) receptor agonist. Plecanatide (brand name Trulance) was approved in January 2017 by the FDA for the treatment of chronic idiopathic constipation (CIC). Plecanatide stimulates intestinal fluid secretions in the gastrointestinal tract to support regular bowel function. Plecanatide, taken orally once daily, works locally in the upper GI tract to stimulate secretion of intestinal fluid and support regular bowel function. Plecanatide is structurally related to human uroguanylin, and similar to uroguanylin, plecanatide functions as a guanylate cyclase-C (GC-C) agonist. Both plecanatide and its active metabolite bind to GC-C and act locally on the luminal surface of the intestinal epithelium. Activation of GC-C results in an increase in both intracellular and extracellular concentrations of cyclic guanosine monophosphate (cGMP). Elevation of intracellular cGMP stimulates secretion of chloride and bicarbonate into the intestinal lumen, mainly through activation of the cystic fibrosis transmembrane conductance regulator (CFTR) ion channel, resulting in increased intestinal fluid and accelerated transit. In animal models, plecanatide has been shown to increase fluid secretion into the gastrointestinal (GI) tract, accelerate intestinal transit, and cause changes in stool consistency. — NCATS
Clinical trial activity
14 trials · 10 clinical orgs · 3 marketing orgs
Earliest trial started Feb 1, 2010 (NCT01053962)
Timeline
2010s
- Jan 1, 2010
Synergy Pharmaceuticals — Earliest Phase 2 Sponsor(trial)
- Jan 1, 2013
Synergy Pharmaceuticals — Earliest Phase 3 Sponsor(trial)
- Jan 19, 2017
Synergy Pharmaceuticals — Earliest FDA Approval
- Jan 19, 2017
Synergy Pharmaceuticals — NDA Secondary Org
- Jan 19, 2017
Salix — NDA Secondary Org
- Jan 19, 2017
Bausch Health Companies — NDA Secondary Org
- Jan 19, 2017
Synergy Pharmaceuticals — NDA Organization
2020s
- Jan 1, 2022
Earliest Phase 1 Sponsor(trial)
Indications
Approved for
Mechanism of action
NPR1 activator
GUCY2C agonist
Approval history
- approvedJan 19, 2017
Chemistry & pharmacology
SMILES
CC(C)C[C@H](NC(=O)[C@@H]1CSSC[C@@H]2NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CCC(=O)O)NC(=O)[C@@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](N)CC(N)=O)CSSC[C@H](NC(=O)[C@H](C)NC(=O)[C@H](C(C)C)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](C(C)C)NC2=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)NCC(=O)N1)C(=O)O- Mol. weight
- 1681.91 g/mol
- Chirality
- Single Stereoisomer
- Inorganic
- No
- Polymer
- No
- Delivery
- Oral
- Availability
- Prescription Only
- Multi-specific
- No
Oral
Yes
Parenteral
No
Topical
No
Sources
- WikipediaPlecanatide ↗
- NCATS7IK8Z952OK ↗
- ChEMBLCHEMBL2103867 ↗
Also known as
- guanilib
- guanilib
- plecanatide
- plecanatide
- plecanatide
- plecanatide
- plecanatide
- plecanatide
- plecanatide
- plecanatide
- sjp-304
- sp-304
- sp-304
- sp-304
- trulance
- trulance
- trulance
- trulance
Clinical trials
| NCT ID | Phase | Start date | Sponsor(s) |
|---|---|---|---|
| NCT05107219 | Early Phase 1 (Phase 1) | Apr 17, 2022 | National Cancer Institute (NCI), Temple University |
| NCT05151328 | Phase 3 | Dec 1, 2021 | Shandong Luoxin Pharmaceutical Group Stock Co., Ltd. |
| NCT03596905 | Phase 2 | Jun 30, 2018 | Synergy Pharmaceuticals |
| NCT03120520 | Phase 2 | Jan 1, 2017 | Synergy Pharmaceuticals |
| NCT02737397 | Phase 2 | Mar 1, 2016 | Clinilabs, JMI Capital Group |
| NCT02706483 | Phase 3 | Jan 1, 2016 | Synergy Pharmaceuticals |
| NCT02493452 | Phase 3 | Jun 1, 2015 | Synergy Pharmaceuticals |
| NCT02387359 | Phase 3 | Dec 1, 2014 | Synergy Pharmaceuticals |
| NCT02122471 | Phase 3 | Apr 1, 2014 | Synergy Pharmaceuticals |
| NCT01982240 | Phase 3 | Nov 1, 2013 | Synergy Pharmaceuticals |
| NCT01919697 | Phase 3 | Aug 1, 2013 | ClinSearch, LLC, INC Research, Synergy Pharmaceuticals |
| NCT01722318 | Phase 2 | Nov 1, 2012 | Oklahoma Foundation for Digestive Research, Synergy Pharmaceuticals |
| NCT01429987 | Phase 2/Phase 3 (Phase 3) | Oct 1, 2011 | Parexel, Synergy Pharmaceuticals |
| NCT01053962 | Phase 2 | Feb 1, 2010 | Synergy Pharmaceuticals |
Organizations
Research & Development (10)
| Organization | Org type | Trials | As lead sponsor | Phases | Earliest year |
|---|---|---|---|---|---|
| Synergy Pharmaceuticals | For profit | 11 | 11 | 2 | 2010 |
| Clinilabs | For profit | 1 | 0 | 1 | 2016 |
| ClinSearch, LLC | For profit | 1 | 0 | 1 | 2013 |
| INC Research | For profit | 1 | 0 | 1 | 2013 |
| JMI Capital Group | For profit | 1 | 1 | 1 | 2016 |
| National Cancer Institute (NCI) | Government | 1 | 1 | 1 | 2022 |
| Oklahoma Foundation for Digestive Research | Academic/Hospital | 1 | 0 | 1 | 2012 |
| Parexel | For profit | 1 | 0 | 1 | 2011 |
| Shandong Luoxin Pharmaceutical Group Stock Co., Ltd. | For profit | 1 | 1 | 1 | 2021 |
| Temple University | Academic/Hospital | 1 | 0 | 1 | 2022 |
Marketing (4)
| Organization | Org type | Relationship | Date |
|---|---|---|---|
| Bausch Health Companies | For profit | NDA2 | Jan 19, 2017 |
| Salix | For profit | NDA2 | Jan 19, 2017 |
| Synergy Pharmaceuticals | For profit | NDA2 | Jan 19, 2017 |
| Synergy Pharmaceuticals | For profit | NDA | Jan 19, 2017 |