OnCo
trialsTrialPositive

ECLIPSE

Curium's PSMA radioligand met its progression endpoint; survival data and an FDA filing are pending.

~400 men; rPFS primary endpoint met (2025); OS maturing; study completion projected 2029; FDA submission plan under discussion.

Setting
PSMA-positive mCRPC after ARPI, taxane-naive: 177Lu-PSMA-I&T (7.4 GBq × 6) vs ARPI switch
Phase
Phase 3
Sponsor
Curium
Registry
Headline result
rPFS significantly improved.
Reported
2025
Enrolled
439
Replication
Consistent with PSMAfore for the pre-chemotherapy setting; OS pending.

Outcomes

1top
In plain words
What these results mean for people, not percentages
439 people took part
Radiographic progression-free survivalprimarysurrogate endpoint
  • Numbers are not recorded here for this endpoint. 177Lu-PSMA-I&T: Met per sponsor; medians pending publication; ARPI switch.
  • This is a surrogate endpoint: it measures the cancer being controlled or absent on scans and tests, which often, but not always, translates into living longer.
  • These results apply to the people the trial enrolled: PSMA-positive mCRPC after ARPI, taxane-naive: 177Lu-PSMA-I&T (7.4 GBq × 6) vs ARPI switch. People in a different situation may not see the same effect.
  • The trial selected people by a biomarker (PSMA); the result should not be assumed for people whose cancer does not have it.

Numbers are from the trial as recorded here; see the source links in the table below. This is orientation, not medical advice: ask your team how closely the trial population matches you.

439 participants enrolled.

Radiographic progression-free survivalprimary

Met per sponsor; medians pending publication

Source
EndpointArmnValueHR (95% CI)pSource
Radiographic progression-free survivalprimary177Lu-PSMA-I&TMet per sponsor; medians pending publicationlink
ARPI switch
Replication
Consistent with PSMAfore for the pre-chemotherapy setting; OS pending.

Connected

2top