VYKAT XR (diazoxide choline)
VYKAT XR helps patients with hyperphagia associated with Prader-Willi syndrome. It is used for both adults and children as young as four years old who struggle with the excessive hunger characteristic of this condition. This medication is prescribed to manage these specific symptoms in the Prader-Willi patient population.
How VYKAT XR Works
While VYKAT XR treats hyperphagia in patients with Prader-Willi syndrome, the exact way it works within the body is currently unknown. Researchers have not yet identified the specific biological mechanism that leads to its therapeutic effects in this patient group.
Development Insights
Details
- Status
- Prescription
- First Approved
- 2025-03-26
- Patent Cliff
- 2035
- Routes
- ORAL
- Dosage Forms
- TABLET, EXTENDED RELEASE
VYKAT XR Approval History
What VYKAT XR Treats
2 indicationsVYKAT XR is approved for 2 conditions since its original approval in 2025. These indications span multiple therapeutic areas including oncology, immunology, and more.
- Hyperphagia
- Prader-Willi Syndrome
VYKAT XR Competitive Set
ProThree rings of competition based on shared molecular targets and treated indications.
Indication competitors
Same indication, different mechanism — what else might this patient receive?
Filters applied: drops same-active-ingredient (505(b)(2) reformulations), route-mismatch (topical vs systemic), and cross-therapeutic-area matches in same-indication rings.
Drugs Similar to VYKAT XR
3 of 6FDA-approved drugs for similar conditions. Compare mechanisms and indications to understand treatment alternatives.
Clinical Trial Registry
3 trials| Trial | Sponsor ID | Phase | Status | Title |
|---|---|---|---|---|
| NCT00901823 | PK010 | Ph 1 | withdrawn | Open-Label, Single- and Multiple-Dose Pharmacokinetic Study of Diazoxide Choline |
| NCT00688857 | PK008 | Ph 1 | completed | Open-label Pharmacokinetic Study of Diazoxide Choline Coated vs. Uncoated Formulations |
| NCT00696475 | PC007 | Ph 2 | completed | Diazoxide Choline in Hypertriglyceridemia |
Active Pipeline
Ongoing clinical trials by development phase
Key Completed Trials
Completed studies with published results, ranked by significance
Trial Timeline
Full development history with FDA approval milestones
Understanding FDA Approval Types
| Count | Type | What it means |
|---|---|---|
| - | ORIG | Original approval - drug first enters market |
| - | SUPPL - Efficacy | New indication (new disease/condition approved) |
| - | SUPPL - Labeling | Label text changes (warnings, dosing updates) |
| - | SUPPL - Manufacturing | Production changes (new facility) |
| - | SUPPL - Chemistry | Formulation changes (new dosage strength) |
Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.
VYKAT XR FDA Label Details
Indications & Usage
FDA Label (PDF)VYKAT XR is indicated for the treatment of Hyperphagia; Prader-Willi Syndrome.
VYKAT XR Patents & Exclusivity
Patents (6 active)
Exclusivity
Pro Intelligence Preview
Deep insights for VYKAT XR
Revenue Insights
- • Quarterly revenue tracking
- • Historical trend analysis
Patent Timeline
- • Cliff: 2035
- • 54 active patents
Trial Analysis
- • 6 total trials
- • Stage: Declining
Competitive Landscape
- • 6 similar drugs
- • Same target/indication analysis
Full approval history • All patents • Revenue trends • Competitor analysis
Data Sources
Data sourced from official FDA and NIH databases. Click links to verify on original sources.
How We Calculate These Metrics
Trial Activity Stage
Measures the current development activity pattern based on trial phases, status, and trends. Important: This measures R&D activity, not commercial lifecycle.
Trial statuses: "Active" means recruiting or ongoing. "Completed" means reached planned endpoint. "Terminated" means stopped early—often due to safety, efficacy, or business reasons.
- Growth: High proportion of early-phase trials (Phase 1/2), active development
- Expansion: Significant Phase 3 activity, approaching or pursuing approvals
- Mature: Substantial Phase 4 post-marketing studies
- Stable: Mixed phase distribution, steady development
- Declining: Low active trial ratio, reduced R&D investment