Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Sodium phenylacetate + sodium benzoate is an intravenous fixed-dose nitrogen-scavenging combination used as adjunctive emergency therapy for acute hyperammonemia and associated encephalopathy in pediatric and adult patients with urea cycle enzyme deficiencies. Phenylacetate conjugates glutamine to form phenylacetylglutamine, while benzoate conjugates glycine to form hippurate; both nitrogen-containing products are eliminated renally, providing alternative pathways for waste-nitrogen excretion when urea-cycle function is deficient. The reference product is marketed as **Ammonul** as a 10%/10% concentrated aqueous injection requiring dilution before intravenous infusion. Takeda developed an intravenous version under the code TAK-123 and completed a Japanese Phase 1 pharmacokinetic and safety study in healthy adults. ([dailymed.nlm.nih.gov](https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=d564f2b1-9fc7-4201-8066-d745ac3a671f))
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on sodium phenylacetate + sodium benzoate.