drug
vandetanib
Marketedupdated 3mo agoby Genzyme Corp
Approvedcommunity read0 votes
🐶 often sniffed alongside
top 4all catalysts(19)
approval · 19
Apr 6, 2011
approval
CAPRELSA (VANDETANIB) — FDA approval
vandetanib
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Jun 22, 2011
approval
CAPRELSA (VANDETANIB) — FDA approval
vandetanib
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Oct 9, 2012
approval
CAPRELSA (VANDETANIB) — FDA approval
vandetanib
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Jul 3, 2013
approval
CAPRELSA (VANDETANIB) — FDA approval
vandetanib
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Nov 27, 2013
approval
CAPRELSA (VANDETANIB) — FDA approval
vandetanib
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Mar 31, 2014
approval
CAPRELSA (VANDETANIB) — FDA approval
vandetanib
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Jul 28, 2016
approval
CAPRELSA (VANDETANIB) — FDA approval
vandetanib
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Feb 24, 2017
approval
CAPRELSA (VANDETANIB) — FDA approval
vandetanib
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May 16, 2017
approval
CAPRELSA (VANDETANIB) — FDA approval
vandetanib
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Oct 12, 2018
approval
CAPRELSA (VANDETANIB) — FDA approval
vandetanib
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Jun 5, 2020
approval
CAPRELSA (VANDETANIB) — FDA approval
vandetanib
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Jun 15, 2020
approval
CAPRELSA (VANDETANIB) — FDA approval
vandetanib
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Mar 28, 2022
approval
CAPRELSA (VANDETANIB) — FDA approval
vandetanib
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Apr 13, 2023
approval
CAPRELSA (VANDETANIB) — FDA approval
vandetanib
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Mar 7, 2024
approval
CAPRELSA (VANDETANIB) — FDA approval
vandetanib
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May 14, 2025
approval
CAPRELSA (VANDETANIB) — FDA approval
vandetanib
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Jun 26, 2025
approval
CAPRELSA (VANDETANIB) — FDA approval
vandetanib
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Sep 23, 2025
approval
CAPRELSA (VANDETANIB) — FDA approval
vandetanib
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Jan 27, 2026
approval
CAPRELSA (VANDETANIB) — FDA approval
vandetanib
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Trials studying vandetanib
- phase3Study to Determine if Contacting Patients With MTC More Frequently Results in Earlier Detection and Treatment of Signs and Symptoms of AEs and Thus a Decrease in the Percentage of Time Patients Experience AEs During First 12 Months on Vandetanib Treatment
- phase3A Study of Selpercatinib (LY3527723) in Participants With RET-Mutant Medullary Thyroid Cancer
- phase4To Compare The Effects Of Two Doses Of Vandetanib In Patients With Advanced Medullary Thyroid Cancer
- phase3An Efficacy Study Comparing ZD6474 to Placebo in Medullary Thyroid Cancer
- phase2Clinical Trial Comparing Gemcitabine and Vandetanib Therapy With Gemcitabine Alone in Pancreatic Carcinoma
- phase2SAFIR02_Breast - Efficacy of Genome Analysis as a Therapeutic Decision Tool for Patients With Metastatic Breast Cancer
- phase3Efficacy Study Comparing ZD6474 in Combination With Pemetrexed and Pemetrexed Alone in 2nd Line NSCLC Patients
- —Observational Study to Evaluate Vandetanib in RET -/+ Patients With Metastatic Medullary Thyroid Cancer
Patent cliff
source: FDA Orange Bookfirst barrier falls
Aug 8, 2028
~2.0 years out
Earliest of all listed patents + FDA exclusivities. Generic / biosimilar entry typically only becomes possible AFTER both patent and exclusivity barriers expire.
patents (2)
- Aug 8, 2028formulationUS 80674272.0y
- Aug 8, 2028formulationUS 80674272.0y
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