IDAMYCIN (idarubicin hydrochloride) by Pfizer is dna, inhibiting nucleic acid synthesis, inhibiting topoisomerase ii activity, and producing dna-damaging free radicals. First approved in 1990.
Drug data last refreshed 15h ago · AI intelligence enriched 6d ago
IDAMYCIN (idarubicin hydrochloride) is a semi-synthetic anthracycline chemotherapy agent administered intravenously as a powder for reconstitution. It intercalates DNA, inhibits topoisomerase II, and generates DNA-damaging free radicals to disrupt nucleic acid synthesis. Primary use is in acute myeloid leukemia (AML) and other hematologic malignancies.
Product approaching loss of exclusivity with moderate competitive pressure (30/100), signaling potential team restructuring and shift toward defense rather than growth.
DNA, inhibiting nucleic acid synthesis, inhibiting topoisomerase II activity, and producing DNA-damaging free radicals.
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Working on IDAMYCIN offers limited growth trajectory given LOE-approaching status and minimal linked job openings. Career value lies in managing a legacy oncology asset, defending market share, and potentially transitioning to combination or niche strategies before generic erosion accelerates.
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
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