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Col-Probenecid (probenecid)
ORLYNVAH combines sulopenem etzadroxil, a penem antibacterial, with probenecid to increase sulopenem's plasma concentration by inhibiting its renal clearance.
Col-Probenecid, also known as probenecid, is a small molecule drug developed by Merck that targets carbonic anhydrase 9. It is classified as a probenecid drug and was FDA approved in 1951 for indications such as articular gout, chronic gouty arthritis, and hyperuricemia. Probenecid is now off-patent and has multiple generic manufacturers. It has a bioavailability of 99% and a half-life of 5.9 hours. As an off-patent drug, it is widely available in the market.
At a glance
| Generic name | probenecid |
|---|---|
| Sponsor | Pfizer Inc. |
| Drug class | probenecid |
| Target | Carbonic anhydrase 9 |
| Therapeutic area | Immunology |
| Phase | FDA-approved |
| First approval | 1951 |
Mechanism of action
ORLYNVAH is a combination drug that includes sulopenem etzadroxil, which fights bacterial infections, and probenecid, which prevents the kidneys from removing sulopenem too quickly. This results in higher levels of sulopenem in the blood, enhancing its effectiveness.
Approved indications
- Uncomplicated UTI
Common side effects
- diarrhea
- nausea
- vulvovaginal mycotic infection
- headache
- vomiting
Drug interactions
- Ketorolac tromethamine
- Ketoprofen
- Indomethacin
- Naproxen
- Methotrexate
- Rifampin
- Lorazepam
- Oral Sulfonylureas
- Valproic Acid
- Sulopenem
Key clinical trials
- Pharmacokinetics of Sulopenem Etzadroxil Plus Probenecid in Adolescents (PHASE1)
- Probenecid Administration for Alcohol Craving and Consumption (PHASE2)
- Improvement of Reproductive Function in Men With Spinal Cord Injury (SCI) (PHASE3)
- Data Analysis for Drug Repurposing for Effective Alzheimer's Medicines - (DREAM) Probenecid vs Allopurinol
- Probenecid (PB) to Treat Hereditary Nephrogenic Diabetes Insipidus (NDI), ADPKD Treated With Tolvaptan, and Severely Polyuric Patients With Previous Lithium Administration (PHASE2)
- The Re-Prosper HF Study (PHASE2,PHASE3)
- Efficacy of Probenecid on Cluster Seizures During Anti Seizure Medication Withdrawal in Presurgical Focal Epilepsy Video-EEG Monitoring (PHASE2)
- Phase 1 Study of the Pharmacokinetics of Amoxicillin in Pregnancy (PHASE1)
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| FDA label | Mechanism, indications, dosing, boxed warnings, drug interactions |
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Col-Probenecid CI brief — competitive landscape report
- Col-Probenecid updates RSS · CI watch RSS
- Pfizer Inc. portfolio CI