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Trial · NCT07913568

Registered outcomes12

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

ListOutcomeTime frameDescription
PrimaryObjective Response Rate (ORR) assessed by the central review
Baseline up to 3 years. Overall Response is assessed every 8 weeks until 24 weeks after initiation of protocol treatment, and every 12 weeks after 25 weeks and after termination. It continues until PD confirmation or post-study treatment initiation.
SecondaryObjective Response Rate (ORR) as assessed by the investigator (site assessment)
Baseline up to 3 years. Overall Response is assessed every 8 weeks until 24 weeks after initiation of protocol treatment, and every 12 weeks after 25 weeks and after termination. It continues until PD confirmation or post-study treatment initiation.
SecondaryProgression-Free Survival (PFS)From baseline up to 3 years
SecondaryOverall Survival (OS)From baseline up to 3 years
SecondaryDisease Control Rate (DCR)From baseline up to 3 years
SecondaryIncidence of adverse eventsFrom baseline up to 3 years
SecondaryIncidence of Adverse ReactionsFrom baseline up to 3 years
SecondaryIncidence of Serious Adverse Events/ Adverse ReactionsFrom baseline up to 3 years
SecondaryDuration of Response (DoR)From baseline up to 3 years
SecondaryTime to Response (TTR)From baseline up to 3 years
SecondaryEORTC QLQ-C30From baseline up to 3 years
The score range is 0-100 (minimum: 0; maximum: 100). Global health status/QOL: Higher standardized scores indicate better outcomes. Symptom scales/items: Higher standardized scores indicate worse outcomes.
SecondaryQLQ-OV28From baseline up to 3 yearsThe score range is 0-100 (minimum: 0; maximum: 100). Symptom scales/items: Higher standardized scores indicate worse outcomes.

Source ClinicalTrials.govtrials-2026-11-12-0.4.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone 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.

For software

Read this list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT07913568/registered