TRUQAP (capivasertib) is a AstraZeneca/Alexion program in Dephosphorylated Phosphatase and Tensin Homolog (dPTEN) Hormone-Sensitive Prostate Cancer (HSPC). The FDA approved it on Jun 12, 2026. 1 FDA decision on record below. Every date links its source.
Indication under review: Dephosphorylated Phosphatase and Tensin Homolog (dPTEN) Hormone-Sensitive Prostate Cancer (HSPC). Sponsor: AstraZeneca/Alexion (AZN). Market-cap tier at the time we tracked it: Large. We track 2 catalyst events for this program: 0 upcoming and 2 in the record. A PDUFA date is the FDA's target date to complete review of a marketing application; a readout is the sponsor's expected date for clinical trial results. What a PDUFA date is · why we do not compare trial results across drugs.
When is TRUQAP (capivasertib)'s next FDA decision or readout?
No upcoming catalyst is on our calendar for TRUQAP (capivasertib); 1 FDA decision is on record below.
What happened at TRUQAP (capivasertib)'s most recent FDA decision?
On Jun 12, 2026 the FDA approved the application. The decision page carries the source document and the measured share-price reaction.
What is TRUQAP (capivasertib) used for?
In our records TRUQAP (capivasertib) is under review or in development for Dephosphorylated Phosphatase and Tensin Homolog (dPTEN) Hormone-Sensitive Prostate Cancer (HSPC).
Who makes TRUQAP (capivasertib)?
AstraZeneca/Alexion (AZN).
Has TRUQAP (capivasertib) been approved by the FDA?
Yes. The FDA approved an application for TRUQAP (capivasertib) on Jun 12, 2026; the decision page linked above carries the source.
Where does this data come from?
FDA announcements, sponsor press releases and SEC filings; every date on this page links its source.
Facts and dates only; not investment advice. Verify against primary FDA, SEC
and company filings. pdufa.bio is not affiliated with the FDA.
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