CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 80 enrolled
Drug / intervention
RO7300490 +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04857138
NCT04857138Phase 1Completed

An Open-Label, Multicenter, Dose-Escalation and Expansion, Phase I Study to Evaluate Safety, Pharmacokinetics, And Anti-Tumor Activity of RO7300490, A Fibroblast Activation Protein-α (FAP) Targeted CD40 Agonist, as Single Agent or in Combination With Atezolizumab in Participants With Advanced and/or Metastatic Solid Tumors

Hoffmann-La Roche·interventional·Posted Apr 23, 2021·Updated Feb 5, 2024

In Brief

A Phase 1 clinical trial evaluating RO7300490 and Atezolizumab for Solid Tumors. Completed, enrolled 80 participants across 11 sites in 5 countries.

Detailed Summary

A study to evaluate the safety, pharmacokinetics and anti-tumor activity of RO7300490 as a single agent or in combination with atezolizumab. The study will consist of 3 parts: \[Part 1\] Dose-Escalation of RO7300490 as a single agent; \[Part 2\] Dose-Escalation of RO7300490 in combination with atezolizumab and \[Part 3\] Dose-Expansion of RO7300490 in combination with atezolizumab in selected cancer types.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSolid Tumors
CountriesDenmark, France, South Korea, Spain, United Kingdom
Collaborators--

Timeline

Phase 1CompletedFinished
20222023202420252026
First PostedApr 23, 2021
Enrollment StartMay 18, 2021
Primary CompletionJan 18, 2024
TodayJul 2, 2026
Enrollment to primary: 2.7 yearsPosted 5.2 years ago

Interventions

RO7300490drug

Participants will receive RO7300490, as described in the Arm Descriptions.

Atezolizumabdrug

Participants will receive Atezolizumab, as described in the Arm Descriptions.