TheraRadar
Data updated: May 26, 2026

VARUBI (rolapitant hydrochloride)

Oncology Approved 2015-09-01

Varubi helps adults undergoing cancer chemotherapy by preventing delayed nausea and vomiting that can occur after treatment. It is used for patients receiving both initial and repeat courses of emetogenic chemotherapy, including highly emetogenic regimens. This medication is typically used in combination with other anti-nausea drugs to provide comprehensive support during cancer care.

Source: FDA Label • TERSERA

How VARUBI Works

This drug works by selectively binding to human substance P/NK1 receptors as a competitive antagonist. By targeting these specific receptors without affecting other systems like NK2 or NK3, it helps block the signals that trigger chemotherapy-induced emesis.

2
Indications
--
Phase 3 Trials
10
Years on Market

Details

Status
Discontinued
First Approved
2015-09-01
Patent Cliff
2032

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Routes
INTRAVENOUS, ORAL
Dosage Forms
EMULSION, TABLET

Companies

Active Ingredient: ROLAPITANT HYDROCHLORIDE

VARUBI Approval History

2016
2017
2018
2019
2020
2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
8 FDA actions from 2015 to 2020
Aug 2020 SUPPL
Label · Labeling
Apr 2018 SUPPL
Label · Labeling
Oct 2017 ORIGINAL
New Form · Type 3 - New Dosage Form

What VARUBI Treats

2 indications

VARUBI is approved for 2 conditions since its original approval in 2015. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Nausea
  • Vomiting
Source: FDA Label

VARUBI Competitive Set

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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 VARUBI

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Clinical Trial Registry

1 trials
Trial Sponsor ID Phase Status Title
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
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Active Pipeline

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Key Completed Trials

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Completed studies with published results, ranked by significance

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Trial Timeline

Full development history with FDA approval milestones

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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.

VARUBI FDA Label Details

Indications & Usage

FDA Label (PDF)

VARUBI is indicated for the treatment of Nausea; Vomiting.

View full patent landscape →
8 OB patents · 5 families · 227 international docs across 36 countries

VARUBI Patents & Exclusivity

Latest Patent: Jul 2032

Patents (8 active)

US9101615 Expires Jul 14, 2032
US8361500 Expires Oct 9, 2029
US8470842 Expires Jan 18, 2029
US7049320 Expires Aug 19, 2028
US7981905 Expires Apr 4, 2027
US8404702 Expires Apr 4, 2027
US8178550 Expires Apr 4, 2027
US7563801 Expires Apr 4, 2027
Source: FDA Orange Book

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Patent Timeline

  • Cliff: 2032
  • 13 active patents

Trial Analysis

  • Clinical trial tracking
  • Development stage analysis

Competitive Landscape

  • 20 similar drugs
  • Same target/indication analysis
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Data Sources

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