TheraRadar
Data updated: Jul 17, 2026

NAVITRUX (fosaprepitant dimeglumine) · AVYXA HOLDINGS

Approved 2026-06-24

NAVITRUX is FDA-approved to treat 2 conditions (same as FOCINVEZ).

1
Indication
--
Phase 3 Trials
0
Years on Market

Details

Status
Prescription
First Approved
2026-06-24
Routes
INTRAVENOUS
Dosage Forms
POWDER

Companies

Active Ingredient: FOSAPREPITANT DIMEGLUMINE

NAVITRUX Approval History

Original
New Indication
New Form
Label Update
1 FDA actions from 2026 to 2026
Jun 2026 ORIGINAL
Update · Type 5 - New Formulation or New Manufacturer

What NAVITRUX Treats

2 indications

NAVITRUX is approved for 2 conditions since its original approval in 2026. These indications span multiple therapeutic areas including oncology, immunology, and more.

Same approved indications as FOCINVEZ (same active ingredient).

Source: FDA Label
📋

Clinical Trial Registry

9 trials
Trial Sponsor ID Phase Status Title
NCT03578081 results posted A221602 NCI-2017-02410, UG1CA189823 Ph 3 completed Olanzapine With or Without Fosaprepitant Dimeglumine in Preventing Chemotherapy Induced Nausea and Vomiting in Cancer Patients Receiving Highly Emetogenic Chemotherapy
NCT04054193 results posted 0517-045 MK-0517-045, 2018-004844-43 Ph 4 completed Safety of a Three-Day Fosaprepitant Regimen for the Prevention of Chemotherapy-Induced Nausea and Vomiting in Pediatric Participants (MK-0517-045)
NCT02732015 results posted 2015-0587 NCI-2016-00801, 2015-0587 Ph 2 terminated Rolapitant Hydrochloride in Preventing Nausea/Vomiting in Patients With Sarcoma Receiving Chemotherapy
NCT01594749 results posted 0517-031 Ph 3 completed Efficacy and Safety of Fosaprepitant Dimeglumine in Preventing Chemotherapy-Induced Nausea and Vomiting (MK-0517-031)
NCT01405924 EVADE results posted 0517-030 Ph 2 terminated Fosaprepitant (MK-0517, EMEND® IV) In Salvage Treatment of Chemotherapy-Induced Vomiting (MK-0517-030)
NCT01649258 1B-11-5 NCI-2012-01170 Ph 1 terminated Fosaprepitant Dimeglumine and Granisetron Transdermal System in Preventing Nausea and Vomiting in Patients With Breast Cancer Undergoing Chemotherapy
NCT00895245 results posted 6862 NCI-2009-01669 Ph 2 terminated Fosaprepitant Dimeglumine, Palonosetron Hydrochloride, and Dexamethasone in Preventing Nausea and Vomiting Caused by Cisplatin in Patients With Stage III or Stage IV Head and Neck Cancer Undergoing Chemotherapy and Radiation Therapy
NCT01031953 results posted CDR0000612580 P30CA069533, OHSU-HEM-08053-L Ph 1, Ph 2 terminated Fosaprepitant Dimeglumine in Treating Patients With Nausea and Vomiting Caused By Chemotherapy
NCT01074697 GAND-emesis GAND-emesis 2009-014691-21 Ph 3 completed Efficacy of Two Antiemetic Regimens in Patients Receiving Radiotherapy and Concomitant Weekly Cisplatin
🔬

Active Pipeline

Pro

Ongoing clinical trials by development phase

Loading...

Key Completed Trials

Pro

Completed studies with published results, ranked by significance

Loading...
📊

Trial Timeline

Full development history with FDA approval milestones

|
Loading...
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.

NAVITRUX FDA Label Details

Indications & Usage

FDA Label (PDF)

NAVITRUX is FDA-approved to treat 2 conditions — same approved indications as FOCINVEZ.

Track NAVITRUX with TheraRadar Pro

Watchlist alerts, full database access, CSV exports across 14,000+ drugs.

Upgrade to Pro

Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.