Ro7247669

Clinical trials are investigating Ro7247669 in several cancer settings, including melanoma, hepatocellular carcinoma, urothelial cancer, and advanced liver cancers. These studies are looking at safety, effectiveness, and response to treatment in different patient groups, mostly in people with untreated or advanced disease.

Table of Contents

Trial overview

The available studies of Ro7247669 are testing it in cancer trials, not as a general medicine article. The trials focus on whether it can help people with different types of cancer and whether the treatment is safe in these study groups.[1][2][3][4]

All four trials listed are interventional studies, which means researchers give a treatment and then measure what happens.[1][2][3][4]

Cancer types being studied

One completed Phase 2 trial studied people with previously untreated unresectable or metastatic melanoma, which means melanoma that could not be removed by surgery or had spread to other parts of the body, and had not been treated before in this setting.[1]

Another completed Phase 1 trial studied surgically resectable hepatocellular carcinoma, which is a liver cancer that can be removed with surgery.[2]

A Phase 2 authorised trial is studying previously untreated locally advanced or metastatic urothelial cancer, meaning cancer of the urinary tract that is either locally advanced or has spread, and has not been treated before in this setting.[3]

Another authorised Phase 1 study is looking at advanced liver cancers, a broad group of later-stage liver cancer cases.[4]

Trial phases and status

The studies include both Phase 1 and Phase 2 trials.[1][2][3][4] Phase 1 trials usually focus on safety and early activity, while Phase 2 trials look more closely at how well a treatment works.[2][3][4]

Two studies are marked Completed, and two are marked Authorised.[1][2][3][4] Completed means the study has finished, while authorised means the study has been allowed to proceed.[1][2][3][4]

The enrollment numbers range from 101 to 309 participants, showing that these are medium-sized cancer studies.[1][2][3][4]

Who can participate

Each study has a specific patient group, so not everyone with cancer can join.[1][2][3][4]

  • People with previously untreated unresectable or metastatic melanoma could be included in the melanoma study.[1]

  • People with surgically resectable hepatocellular carcinoma could be included in the liver cancer surgery study.[2]

  • People with previously untreated locally advanced or metastatic urothelial cancer could be included in the urothelial cancer study.[3]

  • People with advanced liver cancers could be included in the Morpheus-Liver study.[4]

The trial data do not give full detail on all eligibility rules, so the main known factor is the cancer type and whether it is untreated, resectable, advanced, or metastatic.[1][2][3][4]

What the trials measure

The melanoma study measures progression-free survival (PFS), which is the time from randomization until the cancer gets worse or the patient dies during the treatment period or soon after treatment ends.[1]

The hepatocellular carcinoma study measures major pathologic response (MPR) rate, which means how much tumor is left in tissue after treatment and surgery.[2]

The urothelial cancer study mainly measures the incidence and severity of adverse events, which are unwanted medical problems during the study.[3]

The advanced liver cancer study measures objective response rate (ORR), adverse events, changes in vital signs, electrocardiogram (ECG) readings, and targeted laboratory test results.[4]

Treatment combinations in the studies

Ro7247669 is studied alone in some settings and with other cancer treatments in others.[1][3][4]

In the melanoma study, the brief summary says the trial is evaluating Ro7247669 at 600 mg and 1200 mg every 3 weeks, with the main focus on progression-free survival.[1]

In the hepatocellular carcinoma study, Ro7247669 is part of neoadjuvant immunotherapy combinations, meaning treatment given before surgery.[2]

In the urothelial cancer and advanced liver cancer studies, Ro7247669 is included among several immunotherapy-based combinations, showing that researchers are comparing different treatment plans rather than only one drug approach.[3][4]

Trial ID Phase Condition studied Status Enrollment
2023-505672-30-00 Phase 2 Previously untreated unresectable or metastatic melanoma Completed 101
2022-502840-11-00 Phase 1 Surgically resectable hepatocellular carcinoma Completed 143
2023-504027-78-00 Phase 2 Previously untreated locally advanced or metastatic urothelial cancer Authorised 244
2023-506611-17-00 Phase 1 Advanced liver cancers Authorised 309

Ongoing Clinical Trials on Ro7247669

  • Study on the Effectiveness and Safety of TPST-1120 and Drug Combination for Patients with Advanced Liver Cancer

    Recruiting

    1 1 1
    France
  • Study of RO7247669 at Different Doses for People with Previously Untreated Advanced Melanoma that Cannot be Removed by Surgery or Has Spread

    Not recruiting

    1 1
    Investigated drugs:
    Czechia Greece Poland Slovakia Spain
  • Study of RO7247669, Tiragolumab, and Atezolizumab for Patients with Untreated Advanced Urothelial Cancer Ineligible for Platinum Chemotherapy

    Not recruiting

    1 1 1
    Investigated drugs:
    Denmark France Germany Greece Italy Poland +1
  • Study on the Effectiveness and Safety of Bevacizumab, Atezolizumab, and RO7247669 in Patients with Resectable Liver Cancer

    Not recruiting

    1 1 1
    Investigated diseases:
    Austria France Germany Spain

Glossary

  • Interventional study: A study where researchers give a treatment or treatment combination to see what happens.
  • Phase 1: An early trial phase that mainly checks safety and looks for early signs that a treatment may help.
  • Phase 2: A trial phase that looks more closely at how well a treatment works and continues to watch safety.
  • Unresectable: Not able to be removed with surgery.
  • Metastatic: Cancer that has spread from where it started to other parts of the body.
  • Neoadjuvant: Treatment given before the main treatment, often before surgery.
  • Major pathologic response (MPR): A strong cancer response seen in tissue after treatment, usually meaning very little active tumor remains.
  • Progression-free survival (PFS): The length of time during and after treatment that a cancer does not get worse.
  • Objective response rate (ORR): The percentage of patients whose tumors shrink or disappear during treatment.
  • RECIST v1.1: A standard way doctors measure whether tumors have grown, stayed the same, or shrunk in a trial.
  • Adverse events: Unwanted medical problems that happen during a study, whether or not they are caused by the treatment.
  • Cytokine Release Syndrome (CRS): A strong immune reaction that can happen with some treatments and may cause fever and other symptoms.

References

  1. https://clinicaltrials.gov/study/2023-505672-30-00
  2. https://clinicaltrials.gov/study/2022-502840-11-00
  3. https://clinicaltrials.gov/study/2023-504027-78-00
  4. https://clinicaltrials.gov/study/2023-506611-17-00