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Details:

Edurant (rilpivirine) is a human immunodeficiency virus type 1 (HIV-1) specific, non-nucleoside reverse transcriptase inhibitor (NNRTI) indicated in combination with other antiretroviral agents for the treatment of HIV-1 infection.


Lead Product(s): Rilpivirine,Cabotegravir

Therapeutic Area: Infections and Infectious Diseases Product Name: Edurant

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 19, 2024

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Cabenuva is a combination of cabotegravir which inhibits HIV integrase by binding to the integrase active site and blocking the strand transfer step of retroviral DNA integration which is essential for HIV replication and rilpivirine which inhibits HIV-1 reverse transcriptase.


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Cabenuva

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 06, 2024

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  • Development Update

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Vocabria (cabotegravir injection) is an integrase strand transfer inhibitor and used in combination with the Janssen Pharmaceutical Companies of Johnson & Johnson's Rekambys (rilpivirine long-acting injection) for the treatment of HIV-1 infection.


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Vocabria

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 26, 2023

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Cabenuva is a combination of cabotegravir which inhibits HIV integrase by binding to the integrase active site and blocking the strand transfer step of retroviral DNA integration which is essential for HIV replication and rilpivirine which inhibits HIV-1 reverse transcriptase.


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Cabenuva

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable February 23, 2023

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SACT-1 (rilpivirine) is an orally administered repurposed small molecule drug to target neuroblastoma. SACT-1’s mechanism has been investigated to enhance tumor cell death and suppress MYCN expression.


Lead Product(s): Rilpivirine

Therapeutic Area: Oncology Product Name: SACT-1

Highest Development Status: Phase IProduct Type: Small molecule

Partner/Sponsor/Collaborator: Aenco Technologies Limited

Deal Size: $3.0 million Upfront Cash: Undisclosed

Deal Type: Private Placement December 16, 2022

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Vocabria (cabotegravir injection), used in combination with rilpivirine injection is a complete long-acting regimen dosed monthly or every 2-months, for the treatment of HIV-1 in adults.


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Vocabria

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 24, 2022

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BRII-732/BRII-778 combination is currently in Phase 1 development in the U.S. as therapy for human immunodeficiency virus infection that can be administered on weekly basis potentially preferable choice for patients currently receiving once-daily treatment for HIV.


Lead Product(s): Islatravir Prodrug,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: BRII-732

Highest Development Status: Phase IProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 19, 2022

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  • Development Update

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Vocabria/Rekambys (cabotegravir, rilpivirine; marketed as Cabenuva in the US) administered every two months in Europe for the treatment of Long Acting HIV.


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Vocabria

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 12, 2022

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CABENUVA is the first and only complete long-acting HIV-1 treatment regimen, and the first to be made available for eligible adolescents, building on Janssen’s ongoing commitment to fighting HIV and improving HIV treatment options for young people living with HIV.


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Cabenuva

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: ViiV Healthcare

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 29, 2022

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US FDA approval of updated label streamlines the initiation process for the cabenuva is first and only complete long-acting HIV treatment by allowing people to start directly with injections.


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Cabenuva

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: GSK

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 24, 2022

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Details:

US FDA approval for Cabenuva (cabotegravir, rilpivirine), integrase strand transfer inhibitor, updated label streamlines the initiation process for the first and only complete long-acting HIV treatment by allowing people to start directly with injections.


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Cabenuva

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Pfizer Inc

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 24, 2022

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U.S.FDA approval is based on FLAIR week 124 results, which showed there were similar outcomes regarding maintenance of virologic suppression, safety, tolerability and pharmacokinetics in people starting Cabenuva (cabotegravir and rilpivirine) injections.


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Cabenuva

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 24, 2022

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Details:

Cabenuva (cabotegravir, rilpivirine) maintain viral suppression is now approved for administration as few as six times a year for virologically suppressed adults living with HIV without prior treatment failure or resistance.


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Cabenuva

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: GSK

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable February 01, 2022

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Details:

CABENUVA is comprised of two separate injectable medicines, rilpivirine extended-release injectable suspension in a single-dose vial, a product of Janssen Sciences, and ViiV Healthcare’s cabotegravir extended-release injectable suspension in a single dose vial.


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Cabenuva

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: ViiV Healthcare

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable February 01, 2022

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Details:

Cabenuva comprised of, rilpivirine extended-release injectable suspension, and cabotegravir extended-release injectable suspension, offers virologically suppressed adults living with HIV an injectable treatment option administered as few as six times a year.


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Cabenuva

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: ViiV Healthcare

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable February 01, 2022

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ViiV Healthcare’s cabotegravir in combination with Janssen Pharmaceutical's rilpivirine was co-developed as part of a collaboration with Janssen and builds on ViiV Healthcare’s industry-leading portfolio that is centred on delivering innovative medicines for the HIV community.


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Vocabria

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Johnson & Johnson Innovative Medicine

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 28, 2021

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Details:

ATLAS-2M met its primary endpoint at Week 48, demonstrating that the efficacy of long-acting cabotegravir and rilpivirine dosed every 2-months (every eight weeks) was non-inferior to monthly dosing (every four weeks).


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Cabenuva

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Johnson & Johnson Innovative Medicine

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 06, 2021

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Details:

ATLAS-2M 96-week findings for investigational long-acting cabotegravir and rilpivirine administered every 2-months for the treatment of HIV-1 in virologically suppressed adults as well as an analysis of renal and bone outcomes from ATLAS and ATLAS-2M.


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Cabenuva

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Johnson & Johnson Innovative Medicine

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 02, 2021

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Details:

The sNDA seeks to expand Cabenuva’s label to include every 2-months dosing for the treatment of HIV-1 infection in virologically suppressed adults on a stable regimen, with no history of treatment failure, and with no known resistance to cabotegravir or rilpivirine.


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Cabenuva

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable February 24, 2021

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Details:

The safety and efficacy of Cabenuva were established through two randomized, open-label, controlled clinical trials in 1,182 HIV-infected adults who were virologically suppressed (HIV-1 RNA less than 50 copies/milliliter) before initiation of treatment with Cabenuva.


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Cabenuva

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Johnson & Johnson Innovative Medicine

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable January 21, 2021

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Details:

Marketing Authorisation granted by European Commission for ViiV Healthcare’s Vocabria (cabotegravir injection and tablets) to be used with Janssen’s Rekambys (rilpivirine injection) and Edurant (rilpivirine tablets).


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Vocabria

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: ViiV Healthcare

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable December 21, 2020

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Marketing Authorisation granted by European Commission for ViiV Healthcare’s Vocabria (cabotegravir injection and tablets) to be used with Janssen’s Rekambys (rilpivirine injection) and Edurant (rilpivirine tablets).


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Vocabria

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Johnson & Johnson Innovative Medicine

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable December 21, 2020

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Details:

Interim data presented at IDWeek 2020 showed the majority of patient participants continue to find once-monthly injectable cabotegravir plus rilpivirine to be acceptable for treating their HIV and appropriate for their daily lives .


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Vocabria

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 22, 2020

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Details:

Twelve-month findings from the POLAR study showed continued durable viral suppression with no incidence of virologic failure among participants who switched to long-acting injectable cabotegravir and rilpivirine from oral regimen.


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Vocabria

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 22, 2020

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Details:

Regimen is based on co-administration of REKAMBYS® (rilpivirine injection) and ViiV Healthcare’s VOCABRIA® (cabotegravir injection) once every month or once every 2- months to treat HIV-1.


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Vocabria

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 16, 2020

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Details:

ViiV Healthcare announced positive initial findings from the CUSTOMIZE trial, which aims to identify successful methods of implementing the investigational once-monthly, long-acting regimen of cabotegravir and rilpivirine for the treatment of HIV-1 into clinical practice.


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Cabenuva

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable July 04, 2020

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Details:

Comapany to present the final efficacy analysis from the global HPTN 083 study evaluating cabotegravir for HIV prevention.


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Cabenuva

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable July 02, 2020

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Details:

Findings from the ATLAS-2M phase III study showed that the administration of injectable cabotegravir and rilpivirine every two months was as effective and safe as once-monthly administration.


Lead Product(s): Cabotegravir,Rilpivirine

Therapeutic Area: Infections and Infectious Diseases Product Name: Undisclosed

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 09, 2020

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