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Trial · NCT07005128

Registered outcomes14

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryOverall Survival (OS)Up to approximately 3.5 years
PrimaryProgression free survival (PFS) (Blinded Independent Central Review [BICR] Assessed)Up to approximately 3.5 years
SecondaryPFS (Investigator Assessed)Up to approximately 4 years
SecondaryObjective Response (OR)Up to approximately 4 years
SecondaryDisease ControlUp to approximately 4 years
SecondaryDuration of Response (DOR)Up to approximately 4 years
SecondaryPFS Rate6 months, 1 year, and 2 years
SecondaryOS Rate6 months, 1 year, 2 years and 3 years
SecondaryTime to ProgressionUp to approximately 4 years
SecondaryNumber of Participants Who Experience Treatment-emergent Adverse Events (TEAEs)Up to approximately 4 years
SecondaryNumber of Participants Who Experience Treatment-related Adverse EventsUp to approximately 4 years
SecondaryNumber of Participants Who Experience Events of InterestUp to approximately 4 years
SecondarySerum Concentrations of TarlatamabUp to approximately 1 year
SecondaryNumber of Participant Who Develop Anti-Tarlatamab AntibodiesUp to 13 months

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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