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Find Drugs in Development News & Deals for EIDD 2801

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Details:

The licences are applicable for both molnupiravir (API) and finished product in capsules form. It enables the company to launch the product within India as well as export to 104 other countries around the world, Biophore India Pharmaceuticals said in a statement.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: MK-4482

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: The Medicines Patent Pool

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Licensing Agreement January 20, 2022

Details:

Molflu a generic version of the Molnupiravir, is the first oral antiviral medication that helps treat mild to moderate COVID-19 in adults is expected to be available from next week in pharmacies throughout (India).


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: Molflu

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable January 04, 2022

Details:

Emergency-use authorisation recieved from DCGI to manufacture and market oral anti-viral drug Molflu (Molnupiravir) 200mg for treatment of adult patients with Covid19.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: Molflu

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable December 29, 2021

Details:

Cipla Limited, Dr Reddy’s Laboratories Ltd, Emcure Pharmaceuticals, Sun Pharmaceutical Industries Limited and Torrent Pharmaceuticals will collaborate for the clinical trial of the oral anti-viral drug molnupiravir for mild Covid-19 in an outpatient setting in India.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: MK-4482

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Cipla

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Collaboration June 29, 2021

Details:

Fermenta Biotech will exclusively license its biocatalytic technology for synthesis of Molnupiravir (Molflu) and supply its enzyme Candida Antarctica B Lipase (CAL B) to Aurigene. Molnupiravir API manufactured by Aurigene will be utilised by Dr Reddy’s for its formulation.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: Molflu

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Fermenta Biotech Limited

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Licensing Agreement January 21, 2022

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DCGI approved Stripiravir (molnupiravir) an orally administered form of a potent ribonucleoside analog that inhibits the replication of SARS‐CoV‐2 in COVID-19 infection.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: Stripiravir

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable December 28, 2021

Details:

Lagevrio (molnupiravir) is an investigational, orally administered nucleoside analog that accumulates errors in the viral genome leading in inhibition of SARS-CoV-2 replication, the causative agent of COVID-19.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: Lagevrio

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Merck Group

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable February 24, 2023

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Lagevrio (molnupiravir) is an investigational, orally administered nucleoside analog that accumulates errors in the viral genome leading in inhibition of SARS-CoV-2 replication, the causative agent of COVID-19.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: Lagevrio

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 21, 2023

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A preliminary analysis in highly-vaccinated adults mostly <65 years of age, showed no evidence of difference between LAGEVRIO (molnupiravir) added to usual care compared to usual care alone for reduction of hospitalizations and deaths through Day 28.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: Lagevrio

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Ridgeback Biotherapeutics

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 06, 2022

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Analyses of pre-specied exploratory endpoints indicate that a lower proportion of LAGEVRIO (Molnupiravir)-treated participants in MTT population had an acute care visit or a COVID-19-related acute care visit versus placebo-treated participants in the MITT population.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: Lagevrio

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Ridgeback Biotherapeutics

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable June 07, 2022

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Lagevrio (molnupiravir), an investigational oral antiviral medicine, cleared infectious SARS-CoV-2 faster than placebo among patients who had infectious virus at baseline, resulting in no infectious virus detected at Day 3, 5 or 10.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: Lagevrio

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Ridgeback Biotherapeutics

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable April 01, 2022

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The studies used established cell-based assays to evaluate the antiviral activity of molnupiravir and other COVID-19 antiviral agents against SARS-CoV-2 variants of concern, including Omicron.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: MK-4482

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Ridgeback Biotherapeutics

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable January 28, 2022

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Details:

This agreement allows Natco to expand access to COVID-19 medicines in 105 countries in generic name. Under the licence, Natco can set its own price for the generic products it produces, paying a royalty on sales to MSD.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: Molnunat

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: The Medicines Patent Pool

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Licensing Agreement January 20, 2022

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  • Deals

Details:

Under the partnership, Strides and UCL will manufacture Stripiravir (molnupiravir), an orally administered form of a potent ribonucleoside analog that inhibits the replication of SARS‐CoV‐2, in India and Nairobi, Kenya.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: Stripiravir

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Medicines Patent Pool

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Partnership January 20, 2022

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Under the agreement, Merck will allocate up to 3 million courses of molnupiravir to UNICEF throughout the first half of 2022 for distribution in more than 100 low- and middle-income countries following regulatory authorizations.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: MK-4482

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: United Nations Children’s Fund

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Agreement January 18, 2022

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Molnulup (Molnupiravir), Clinical data suggests that it is effective on patients with co-morbidities also, has been given emergency use authorization by the DCGI for treatment of adult patients with Covid-19, with SpO2 > 93%.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: Molnulup

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable January 07, 2022

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Molnaflu (Molnupiravir), inhibits the replication of certain RNA viruses used for the treatment of adult patients with COVID-19, with SpO2 >93 percent and who have a high risk of progression of the disease including hospitalization or death.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: Molnaflu

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable January 06, 2022

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Mankind pharma launched Molulife (Molnupiravir) developed by MSD and Ridgeback Biotherapeutics by next week, It is also expected that Cipla, Sun pharma, and DRL will also release Molnupiravir in the coming weeks for the treatment of patients with severe COVID19.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: Molulife

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable January 05, 2022

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DCGI approved the launching of MOLENTOD™ (Molnupiravir), based on the review of clinical data of molnupiravir for treatment of adult patients with Covid-19, with SpO2 > 93% and who have high risk of progression of the disease including hospitalisation or death.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: Molentod

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable January 05, 2022

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Cipmolnu® (Molnupiravir 200mg), first oral antiviral approved by the UK MHRA for the treatment of mild-to-moderate COVID-19 receives EUA by permission by the Drug Controller General of India.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: Cipmolnu

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable December 28, 2021

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Molnupiravir is the first COVID-19 drug authorised by the Drugs Controller General of India (DCGI) for the treatment of COVID-19 infection in adults who have high risk of progression of the disease including hospitalisation or death.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: Molnunat

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable December 28, 2021

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The approval is based on positive results from a planned interim analysis from Phase 3 MOVe-OUT clinical trial by Japan’s Ministry of Health, Labor and Welfare, in Japan LAGEVRIO® (molnupiravir) is planned trademark for molnupiravir.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: MK-4482

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Ridgeback Biotherapeutics

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable December 24, 2021

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This agreement is part of Merck’s commitment to make this investigational medicine widely available globally, if approved for use by regulatory agencies. Molnupiravir is being developed by Merck in collaboration with Ridgeback Biotherapeutics.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: MK-4482

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Merck & Co

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Agreement December 06, 2021

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Merck’s submission to the FDA for EUA is based on the positive results of Molnupiravir an investigational oral antiviral medicine, for the treatment of mild to moderate COVID-19 in adults.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: MK-4482

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Ridgeback Biotherapeutics

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable November 30, 2021

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Molnupiravir investigational, orally administered form of a potent ribonucleoside analog that inhibits the replication of SARS-CoV-2, the causative agent of COVID-19.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: MK-4482

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Ridgeback Biotherapeutics

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable November 26, 2021

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Molnupiravir works by interfering with the replication of virus. This prevents it from multiplying, keeping virus levels low in the body and therefore reducing the severity of the disease.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: Molnupiravir-Generic

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable November 09, 2021

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MK-4482 or EIDD-2801 (Molnupiravir) is an investigational, orally administered form of a potent ribonucleoside analog that inhibits the replication of SARS-CoV-2, the causative agent of COVID-19.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: MK-4482

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Ridgeback Biotherapeutics

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable November 04, 2021

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Details:

Molnupiravir is an investigational medicine developed by US based pharma firm Merc used to treat SARS-CoV-2 infection. In India, Merck Pharma Company had signed licensing agreements with various Indian pharma firms like Cipla, Dr Reddy’s, Emcure, Hetero labs and Sun Pharma.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: MK-4482

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Hetero Biopharma

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 30, 2021

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In order to cater to the unmet medical needs of the nation for a front-end cure to SARS-CoV-2 infection, Optimus is well prepared to ensure manufacturing and distribution of Molnupiravir efficiently and effectively.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: Undisclosed

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: JSS Research

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 28, 2021

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Under the terms of the agreement, MPP, through the license granted by Merck, will be permitted to further license non-exclusive sublicenses to manufacturers and diversify the manufacturing base or WHO-prequalified molnupiravir to countries covered by the MPP License.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: EIDD-2801

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Merck & Co

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Licensing Agreement October 27, 2021

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Details:

Molnupiravir is an investigational, orally administered form of a potent ribonucleoside analog that inhibits the replication of SARS-CoV-2, the causative agent of COVID-19.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: MK-4482

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Ridgeback Biotherapeutics

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 25, 2021

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The funding will be allocated based on consultations with partners, and will support the range of activities required to develop and manufacture generic versions of the drug, molnupiravir, which is being developed by Merck & Co in collaboration with Ridgeback Biotherapeutics.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: EIDD-2801

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Bill & Melinda Gates Foundation

Deal Size: $120.0 million Upfront Cash: Undisclosed

Deal Type: Funding October 20, 2021

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The interim analysis of the medicine showed that 7.3% of patients who received molnupiravir were hospitalised through 29 days as compared with 14.1% of placebo-treated patients who were hospitalised or died. Placebo is a dummy pill that has no therapeutic effect.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: MK-4482

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 08, 2021

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Merck has selected Carbon Health to participate in two double-blinded phase III International clinical trials to test the effectiveness of a new COVID-19 antiviral treatment pill, molnupiravir for both treatment and prophylaxis indications.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: MK-4482

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Merck & Co

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Partnership September 30, 2021

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MOVe-AHEAD is a phase 3 multicenter, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of orally administered molnupiravir compared to placebo in preventing the spread of SARS-CoV-2, the virus that causes Covid-19, within households.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: MK-4482

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Ridgeback Biotherapeutics

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 01, 2021

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Molnupiravir is a potent ribonucleoside analog with antiviral activity against SARS-CoV-2 – prophylaxis, treatment and prevention of transmission – and SARS-CoV-1 (the virus that caused the 2003 SARS outbreak) and MERS.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: MK-4482

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Ridgeback Biotherapeutics

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable August 17, 2021

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Molnupiravir (EIDD-2801/MK-4482) is an investigational, orally bioavailable form of a potent ribonucleoside analog that inhibits the replication of multiple RNA viruses including SARS-CoV-2, the causative agent of COVID-19.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: MK-4482

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Ridgeback Biotherapeutics

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable July 12, 2021

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Molnupiravir is currently being evaluated in a Phase 3 clinical trial, the MOVe-OUT study, for the treatment of non-hospitalized patients with laboratory-confirmed COVID-19 and at least one risk factor associated with poor disease outcomes.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: EIDD-2801

Highest Development Status: Phase II/ Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: US Government

Deal Size: $1,200.0 million Upfront Cash: Undisclosed

Deal Type: Agreement June 09, 2021

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Molnupiravir is an experimental drug having antiviral properties and is currently under clinical-stage study for COVID treatment.


Lead Product(s): Molnupiravir

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 May 25, 2021

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Details:

Under this licensing deal, Hetero will be allowed to expand access of Molnupiravir in India and in other low-and middle-income countries (LMICs), following the approvals for emergency use authorization by local regulatory agencies.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: MK-4482

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Hetero Drugs

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Licensing Agreement April 27, 2021

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Pre-clinical data have shown that Molnupiravir has broad anti-influenza activity, including highly potent inhibition of SARS-CoV-2 replication. Patients treated with Molnupiravir achieved response within 5 days of therapy.


Lead Product(s): Molnupiravir

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 April 26, 2021

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MK-4482, delivered orally, is now in human clinical trials. Remdesivir, an antiviral drug already approved by the U.S. Food and Drug Administration for use against COVID-19, must be provided intravenously, making its use primarily limited to clinical settings.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: MK-4482

Highest Development Status: Phase II/ Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable April 16, 2021

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The companies today reported findings on one secondary objective from the Phase 2a study, showing a reduction in time (days) to negativity of infectious virus isolation in nasopharyngeal swabs from participants with symptomatic SARS-CoV-2 infection.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: MK-4482

Highest Development Status: Phase II/ Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Ridgeback Biotherapeutics

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 06, 2021

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  • Development Update

Details:

Scientists at the Georgia State University Institute for Biomedical Sciences in the US have discovered a new antiviral drug, MK-4482/EIDD-2801 (Molnupiravir), for treating SARS-CoV-2 infection by completely suppressing virus transmission within 24 hours.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: MK-4482

Highest Development Status: Phase II/ Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Merck & Co

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable December 03, 2020

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  • Development Update

Details:

The University of Liverpool, Liverpool School of Tropical Medicine and Southampton Clinical Trials Unit have launched an innovative COVID-19 drug testing platform, AGILE, in the hope of accelerating the development of the most promising therapies.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: EIDD-2801

Highest Development Status: Phase I/ Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable July 08, 2020

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AGILE will test multiple potential therapeutics, and EIDD-2801 was selected to be the first oral anti-viral to be studied in the AGILE platform.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: EIDD-2801

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable July 07, 2020

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Companies Collaborated for advance the development of EIDD-2801, an investigational orally-available antiviral agent currently in early clinical development for the treatment of patients with COVID-19.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: EIDD-2801

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Ridgeback Biotherapeutics

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Collaboration July 01, 2020

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EIDD-2801 is an oral nucleoside analogue that has demonstrated extraordinarily favorable tolerability in Phase 1 at all doses tested.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: EIDD-2801

Highest Development Status: Phase IIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable June 19, 2020

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Under terms of the agreement, Merck, through a subsidiary, will gain exclusive worldwide rights to develop and commercialize EIDD-2801 and related molecules.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: Undisclosed

Highest Development Status: Phase IProduct Type: Small molecule

Partner/Sponsor/Collaborator: Merck & Co

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Licensing Agreement May 26, 2020

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EIDD-2801 has been shown to treat MERS and SARS (two severe coronavirus infections) in animals when given after an infection has been established.


Lead Product(s): Molnupiravir

Therapeutic Area: Infections and Infectious Diseases Product Name: Undisclosed

Highest Development Status: PreclinicalProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable April 13, 2020

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