Drug ID:Drug165
Drug Name:Cobitolimod
CID:121492440
DrugBank ID:DB14819
Modality:Small Molecule
Groups:NULL
US Approved:NULL
Other Approved:NULL
Identifier: NCT01493960, , NCT05404074, , NCT04985968, , NCT03178669
Molecular Formula:C185H233N73O106P18S6
Molecular Weight:5925.0 g/mol
Isomeric SMILES:CC1=CN(C(=O)NC1=O)[C@H]2C[C@@H]([C@H](O2)COP(=O)(O)O[C@H]3C[C@@H](O[C@@H]3COP(=O)(O)O[C@H]4C[C@@H](O[C@@H]4COP(=O)(O)O[C@H]5C[C@@H](O[C@@H]5COP(=O)(O)O[C@H]6C[C@@H](O[C@@H]6COP(=O)(O)O[C@H]7C[C@@H](O[C@@H]7COP(=S)(O)O[C@H]8C[C@@H](O[C@@H]8COP(=S)(O)O[C@H]
Synonyms:Cobitolimod; Kappaproct; Cobitolimod [INN]; Cobitolimod [USAN]; Cobitolimod [WHO-DD]; DIMS 0150; Cobitolimod [USAN:INN:WHO-DD]; IDX 0150; UNII-328101264R; WHO 10066
Phase 0: 0
Phase 1: 0
Phase 2: 0
Phase 3: 0
Phase 4: 0
Description:NULL

Molecular Structure

No molecular structure data available

Knowledge Graph

dtIDCIDCompound NameGene IDGene NameSpeciesPubMed IDsAction
No data available

  • No data available

Phase Distribution
Phase Description
  • Phase 0: Exploratory trials to assess drug behavior in humans
  • Phase 1: Safety trials to determine safe dosage range
  • Phase 2: Efficacy trials to evaluate therapeutic effects
  • Phase 3: Large-scale trials to confirm efficacy and safety
  • Phase 4: Post-marketing surveillance for long-term safety and efficacy

Trial IDTitlePhaseStatusSponsorIndicationsInterventions
NCT05404074 Pharmacokinetics of Cobitolimod Enemas in Participants With Active Ulcerative Colitis PHASE1 UNKNOWN InDex Pharmaceuticals Ulcerative Colitis DRUG: Cobitolimod 500mg Details
NCT04985968 The Efficacy and Safety of Cobitolimod in Participants With Moderate to Severe Active Left-Sided Ulcerative Colitis PHASE3 TERMINATED InDex Pharmaceuticals Ulcerative Colitis DRUG: Cobitolimod 250 mg|DRUG: Cobitolimod 500 mg… Details
NCT03178669 The Efficacy of Cobitolimod in Patients With Moderate to Severe Active Ulcerative Colitis PHASE2 COMPLETED InDex Pharmaceuticals Ulcerative Colitis DRUG: cobitolimod|DRUG: Placebo Details
NCT01493960 The Efficacy and Safety of Cobitolimod (Kappaproct®) in Chronic Active Treatment Refractory Ulcerative Colitis Patients PHASE3 COMPLETED InDex Pharmaceuticals Colitis, Ulcerative DRUG: Cobitolimod|DRUG: Placebo Details
EUCTR2021-002549-13-SK A Randomised Double-Blind Placebo-Controlled Phase III Clinical Study to Evaluate the Efficacy and Safety of Cobitolimod as an Induction and Maintenance Therapy in Participants with Moderate to Severe Active PHASE3 Not Recruiting InDex Pharmaceuticals AB Moderate to Severe left-sided Active Ulcerative C… Product Name: CobitolimodPharmaceutical Form: Rec… Details

Disease IDDisease NameDefinitionCategoryRelated DrugsMechanism
No data available

Strategy IDTherapeutic StrategySynonymsRelated DrugsMechanism
No data available

Cobitolimod for moderate-to-severe, left-sided ulcerative colitis (CONDUCT): a …

PMID: 33031757
Year: 2020
Relationship Type: Treatment Score: 6.5

BACKGROUND: Cobitolimod is a topically administered, DNA-based oligonucleotide that activates Toll-like receptor 9 (TLR9), and previous research has …

The TLR9 Agonist Cobitolimod Induces IL10-Producing Wound Healing Macrophages a…

PMID: 31630153
Year: 2020
Relationship Type: Treatment Score: 6.5

BACKGROUND AND AIMS: The topically applied Toll-like receptor 9 [TLR9] agonist cobitolimod is a first-in-class DNA-based oligonucleotide with demonst…