Table 6.
Chemical and clinical characteristics of drugs approved for other gastrointestinal indications and currently investigated for constipation-predominant irritable bowel syndrome
| Itopride | Neomycin/Rifaximin | |
| Brand name | Ganaton® | Neomycin: Neo-Fradin® |
| Rifaximin: Xifaxan® | ||
| Chemical structure | Benzamide derivative | Neomycin: aminoglycoside |
| Rifaximin: semisynthetic antibiotic based on rifampicin | ||
| Mechanism of action | Dopamine D2 antagonist and acetylcholinesterase inhibitor | Neomycin: inhibition of protein synthesis |
| Rifaximin: inhibition of bacterial RNA synthesis | ||
| Pharmacodynamic effects | Gastrokinetic; | Eradication of methane; accelerated intestinal transit (?) |
| Acceleration of intestinal transit (?) | ||
| Most common adverse events | Diarrhea | Neomycin: |
| Headache | Neurotoxicity | |
| Hyperprolactinemia | Ototoxicity | |
| Nephrotoxicity | ||
| Rifaximin: | ||
| Headache | ||
| Nausea | ||
| Dizziness | ||
| Fatigue | ||
| Approval status/stage of development | Approved in Japan for functional dyspepsia; | FDA-approved for hepatic encephalopathy and traveler’s diarrhea; |
| Phase 2 RCT in IBS-C completed in the United States | Phase 2 efficacy RCT in methane + IBS-C patients, comparing neomycin vs combination rifaximin and neomycin (completed) |
FDA: Food and Drug Administration; IBS-C: Constipation-predominant irritable bowel syndrome; RCT: Randomized controlled trial.