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Medivir AB (SE:MVIR)
:MVIR
Sweden Market
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Medivir AB (MVIR) Drug Pipeline

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Drug Name
Condition
Stage
Status
Study Name
Trial Start Date
Article
Miv-818 (Fostroxacitabine Bralpamide) + Pembrolizumab, Miv-818 (Fostroxacitabine Bralpamide) + Lenvatinib
Hepatocellular Carcinoma, Liver Metastases, Intrahepatic Cholangiocarcinoma
Phase I/II
Completed
A Study to Evaluate MIV-818 in Patients With Liver Cancer Manifestations
Nov 07, 2018
Miv-711
Healthy
Phase I
Completed
A Bioavailability Study of MIV-711 Oral Formulations in Healthy Volunteers
Jan 22, 2018
Miv-711
Osteoarthritis, Knee
Phase II
Completed
A Study to Evaluate Safety and Tolerability of MIV-711 in Osteoarthritis Patients
Dec 22, 2016
Miv-711
Osteoarthritis, Knee
Phase II
Completed
A Study to Evaluate the Efficacy, Safety and Tolerability of MIV-711 in Osteoarthritis Patients
Mar 07, 2016
Pembrolizumab, Birinapant
Solid Tumors
Phase I/II
Terminated
Dose-escalation Study of Birinapant and Pembrolizumab in Solid Tumors
Oct 21, 2015

FAQ

What are the FDA phases for drug approval?
The FDA approval process for new drugs is divided into several phases:
a. Preclinical testing
b. Phase 1 – Safety and dosage
c. Phase 2 – Effectiveness and side effects
d. Phase 3 – Confirmation of effectiveness, monitoring of adverse reactions, and comparison with existing treatments
e. Phase 4 – Post-marketing studies to track long-term safety and effectiveness
    What is a clinical trial?
    A clinical trial is a carefully designed study in which researchers test a drug, treatment, or medical device in people to evaluate its safety, effectiveness, and potential side effects. These trials are essential for determining whether a new treatment should be approved for widespread use.
      What drugs does Medivir AB (MVIR) have in its pipeline
      MVIR is currently developing the following drugs: Miv-818 (Fostroxacitabine Bralpamide) + Pembrolizumab, Miv-818 (Fostroxacitabine Bralpamide) + Lenvatinib, Miv-711, Miv-711. These drug candidates are in various stages of clinical development as the company works toward FDA approval.
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