Trial · NCT07905924
Registered outcomes15
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 15 of 15
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Parts 1A and 1B: Incidence and Severity of Adverse Events (AEs) | From first dose up to approximately 5 years | |
| Primary | Part 2: Incidence and Severity of AEs | From first dose up to approximately 5 years | |
| Primary | Parts 3A, 3B and 3C: Incidence and Severity of AEs | From first dose up to approximately 5 years | |
| Primary | Parts 1A and 1B: Incidence of Dose-limiting Toxicities (DLTs) | From Cycle 1 Day 1 (C1D1) until C1D21 (Cycle 1 = 21 days) | |
| Primary | Part 3A: Incidence of DLTs | From C1D1 until C1D21 (Cycle 1 = 21 days) | |
| Primary | Parts 3B and 3C: Incidence of DLTs | From C1D1 until C1D28 (Cycle 1 = 28 days) | |
| Primary | Parts 1A and 1B: Recommended Dose for Expansion (RDE) of RO7836748 Monotherapy | Up to approximately 5 years | |
| Primary | Parts 3A, 3B, 3C: RDE of RO7836748 in Combination With Other Anti-Cancer Therapies | Up to approximately 5 years | |
| Secondary | Parts 1A, 1B and 2: Plasma Concentrations of RO7836748 and its Metabolites as Monotherapy | Up to approximately 5 years | |
| Secondary | Parts 3A, 3B and 3C: Plasma Concentrations of RO7836748 and its Metabolites in Combination With Other Anti-Cancer Therapies. | Up to approximately 5 years | |
| Secondary | All Parts: Objective response rate (ORR) | Up to approximately 5 years | |
| Secondary | All Parts: Duration of response (DoR) | Up to approximately 5 years | |
| Secondary | All Parts: Disease control rate (DCR) | Up to approximately 5 years | |
| Secondary | All Parts: Progression-free survival (PFS) | Up to approximately 5 years | |
| Secondary | All Parts: Overall survival (OS) | Up to approximately 5 years |
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.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT07905924/registered