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Trial · NCT06350006

Registered outcomes11

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

ListOutcomeTime frameDescription
PrimaryIncidence and severity of AEUp to follow-up period, approximately 24 monthsPhase 1b
PrimaryDose Limiting Toxicity (DLT)approximately 24 monthsPhase 1b
PrimaryMaximal Tolerable Dose (MTD)approximately 24 monthsPhase 1b
PrimaryPhase III Recommended Dose (RP3D)approximately 24 monthsPhase 1b
PrimaryProgression-free survival (PFS) assessed by blind Independent Center Review (BICR) based on RECIST 1.1 criteriaapproximately 36 monthsPhase 3
SecondarySHR-A1904 toxin binding antibodyapproximately 24 monthsPhase 1b
SecondarySHR-A1904 Total antibodyapproximately 24 monthsPhase 1b
SecondaryImmunogenicity indicators of SHR-A1904: drug resistant antibody (ADA) and neutralizing antibody (NAb)approximately 24 monthsPhase 1b
SecondaryExpression level of CLDN18.2 in tumor tissuesapproximately 24 monthsPhase 1b
SecondaryOverall survival (OS)approximately 36 monthsPhase 3
SecondaryIncidence and severity of AEapproximately 36 monthsPhase 3

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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GET https://conductscience.org/api/trials/v1/NCT06350006/registered