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Last reviewed 2026-06-10 · How we verify

suspected recurrence based on elevated serum prostate-specific antigen (PSA) level — Treatment Landscape & Competitive Intelligence

Name: Drug Landscape Pharmaceutical Database
Creator: Drug Landscape
Published: 2026-01-01
License: https://creativecommons.org/licenses/by/4.0/

suspected recurrence based on elevated serum prostate-specific antigen (PSA) level (disease) competitive landscape: 1 marketed treatments tracked, 0 Phase 3 candidates, 0 Phase 2 candidates. Recent regulatory actions and upcoming PDUFA dates across the entire treatment set.

1 marketed 0 Phase 3 0 Phase 2 Live · 30-min refresh

Marketed treatment landscape

Approved drugs treating suspected recurrence based on elevated serum prostate-specific antigen (PSA) level, deduplicated by molecule. See the full disease page for line-of-therapy detail.

Drug	Generic	Sponsor	Class	Target	Line of therapy	First approval
Posluma	FLOTUFOLASTAT	Blue Earth	Radioactive Diagnostic Agent [EPC]			2025-01-01

Phase 3 pipeline

No Phase 3 pipeline candidates tracked.

Phase 2 pipeline

No Phase 2 pipeline candidates tracked.

Recent regulatory actions (last 90 days)

No regulatory actions in the last 90 days for this treatment set.

Upcoming PDUFA dates (next 180 days)

No PDUFA dates in the next 180 days for this treatment set.

Sponsor landscape

Blue Earth · 1 drug in suspected recurrence based on elevated serum prostate-specific antigen (PSA) level

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Every new regulatory action, PDUFA date, or trial completion in suspected recurrence based on elevated serum prostate-specific antigen (PSA) level:

Cite this brief

Drug Landscape (2026). suspected recurrence based on elevated serum prostate-specific antigen (PSA) level — Treatment Landscape & Competitive Intelligence Brief. https://druglandscape.com/ci/disease/suspected-recurrence-based-on-elevated-serum-prostate-specific-antigen-psa-level. Accessed 2026-06-10.

suspected recurrence based on elevated serum prostate-specific antigen (PSA) level full disease profile — treatment pathway, diagnostics, guidelines
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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing