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Clinical Impact and Utility of Digital Health Solutions in Participants Receiving Systemic Treatment in Clinical Practice
- Cancer
Please note that the recruitment status of the trial at your site may differ.
Trial Status:
Recruiting
This trial runs in
Cities
- Aarau
- Aschaffenburg
- Barcelona
- Birtinya
- Concord
- Genève
- Graz
- Jaén
- Klagenfurt am Wörthersee
- Málaga
- Palma
- prilly
- Stade
- Troisdorf
- València
- Wuppertal
- Zaragoza
- Zürich
Trial Identifier:
NCT05694013 MO42720
Trial Summary
This study will evaluate the clinical impact and utility of digital health solutions (DHS) on health outcomes and health-care resource utilization in people receiving systemic anti-cancer treatment (approved or non-approved) in clinical practice.
Hoffmann-La Roche
Sponsor
Phase 2/Phase 3
Phase
NCT05694013,MO42720
Trial Identifier
All
Gender
≥18 Years
Age
No
Healthy Volunteers
1. Why is the MO42720 clinical trial needed?
Digital monitoring of a person’s disease- or treatment-related symptoms and health during treatment may improve treatment results, reduce the number of serious side effects and help doctors and patients to manage symptoms more effectively. A Digital Patient Monitoring system is a web- and app-based electronic system that allows people with cancer to provide information on how they are coping with disease and treatment to their clinics’ care team in a structured and regular way. This clinical trial aims to assess how well Digital Patient Monitoring works to improve health outcomes in people receiving anti-cancer treatment and reduce the use of healthcare resources.
2. How does the MO42720 clinical trial work?
This clinical trial is recruiting people who are being given anti-cancer treatment. The people who take part in the trial are known as ‘participants’. The trial will test the patient monitoring system in groups of participants (known as ‘cohorts’) with different types of cancers or who are receiving different types of treatments. People can take part in:
- Cohort A if they are being treated with atezolizumab for lung cancer (non-small cell lung carcinoma [NSCLC] that has spread in the body or extensive-stage small-cell lung carcinoma) or liver cancer (hepatocellular carcinoma) that has grown or spread in the body or cannot be removed with surgery.
- Cohort B if they are being treated with atezolizumab for lung cancer (NSCLC) that contains a protein called PD-L1, and they have undergone surgery to remove the tumour and completed chemotherapy.
Throughout the trial, half of the participants in Cohort A and all participants in Cohort B will be asked to complete weekly questionnaires on disease- or treatment-related symptoms they have using the Digital Patient Monitoring system, via an app installed on their internet-capable device (computer or mobile phone) or via a web browser. Participants who are not selected to use the patient monitoring app will be able to report symptoms according to normal practice in their local area. All participants in Cohorts A and B will be given access to a second app, to report on their health-related quality of life and impact of symptoms on daily life every 7 days. Participants in Cohort A will be given anti-cancer treatment according to normal practices in the area where they live. Participants in Cohort B will be given an experimental anti-cancer treatment that is not yet approved by health authorities, starting with treatment at the hospital for the first three cycles, and then continuing with treatment at home (by a trained nurse). The clinical trial doctor will see them regularly to check how the participant responds to the treatment and any side effects they may have. The total time in the clinical trial will be up to about 1 and a half years depending on the type of cancer and treatment being given. Participants will be seen at a follow-up visit about 1 month after their last dose and contacted by telephone after 3 months to check on their health. Participants can stop trial treatment and/or stop using the Digital Patient Monitoring system and leave the clinical trial at any time.
3. What are the main endpoints of the MO42720 clinical trial?
The main clinical trial endpoints (the main results measured in the trial) depend on the cohort:
- Cohort A: How participants’ symptoms interfere with daily life at 3 months after the start of the trial
- Cohort B: How many participants choose to receive treatment at home when combined with the use of the patient monitoring app, 4 months after the start of the trial
Other clinical trial endpoints include the:
- Number of emergency or unscheduled visits to hospital due to symptoms/side effects
- Number and seriousness of side effects
- Number of people who pause, change the dose of or stop anti-cancer treatment due to side effects
- Change in quality of life throughout the trial
4. Who can take part in this clinical trial?
People can take part in this trial if they are at least 18 years old, meet the criteria to join a cohort in this trial and have an email address, access to an internet-capable device (smartphone, tablet or PC) and access to an internet connection. People may not be able to take part in this trial if they have a physical or mental condition that prevents them from using the apps provided or have/had certain cancers or certain medical conditions such as long-term infections. Women who are pregnant or breastfeeding or are planning to become pregnant during or shortly after the trial will not be able to take part.
5. What treatment will participants be given in this clinical trial?
Everyone will be given anti-cancer treatment and support from their care team with or without the use of the patient monitoring app. When the patient monitoring app is provided to half of a cohort (such as for Cohort A), they will have an equal chance of being placed in either group.
6. Are there any risks or benefits in taking part in this clinical trial?
The safety or effectiveness of the experimental treatment or use may not be fully known at the time of the trial. Most trials involve some risks to the participant. However, it may not be greater than the risks related to routine medical care or the natural progression of the health condition. People who would like to participate will be told about any risks and benefits of taking part in the clinical trial, as well as any additional procedures, tests or assessments they will be asked to undergo. All of these will be described in an informed consent document (a document that provides people with the information they need to decide to volunteer for the clinical trial).
Risks associated with the clinical trial drugs and patient monitoring app
Participants may have side effects (an unwanted effect of a drug or medical treatment) from the drugs used in this clinical trial. Side effects can be mild to severe, even life-threatening, and vary from person to person. Participants will be closely monitored during the clinical trial; safety assessments will be performed regularly. Participants will be told about the known side effects of anti-cancer treatment, and possible side effects based on human and laboratory studies or knowledge of similar drugs. Anti-cancer treatment will be given as an infusion into a vein (intravenous infusion) in Cohort A, or an injection under the skin (subcutaneous injection) in Cohort B. Participants will be told about any known side effects of anti-cancer treatment, any known risks of the patient monitoring app and where relevant, potential risks based on human and laboratory studies or knowledge of similar devices.
Potential benefits associated with the clinical trial
Participants' health may or may not improve from participation in the clinical trial. Still, the information collected may help other people with similar medical conditions in the future.
For more information about this clinical trial see the For Expert tab on the specific ForPatients page or follow this link to ClinicalTrials.gov: https://clinicaltrials.gov/ct2/show/NCT05694013
Trial Summary
This study will evaluate the clinical impact and utility of digital health solutions (DHS) on health outcomes and health-care resource utilization in people receiving systemic anti-cancer treatment (approved or non-approved) in clinical practice.
Hoffmann-La Roche
Sponsor
Phase 2/Phase 3
Phase
NCT05694013,MO42720
Trial Identifier
Roche DPM Module, Atezolizumab SC, Local SOC support
Treatments
Cancer
Condition
Official Title
Interventional Platform Study Investigating the Impact of Digital Health Solutions on Health Outcomes and Health-Care Resource Utilization in Participants Receiving Systemic Treatment in Clinical Practice
Eligibility Criteria
All
Gender
≥18 Years
Age
No
Healthy Volunteers
Inclusion Criteria
Inclusion Criteria: All Participants
- Email address, access to an internet-capable device (smartphone, tablet, or PC), and access to an internet connection
Inclusion Criteria: Cohort A
- Histologically confirmed diagnosis for mNSCLC, ES-SCLC, or HCC (Child Pugh A)
- Systemic therapy naive
- Prescribed an atezolizumab IV regimen
- Easter Cooperative Oncology Group (ECOG) Performance Status of 0, 1, or 2
Inclusion Criteria: Cohort B
- Complete resection of a histologically or cytologically confirmed Stage IIB-IIIB (T3-N2) NSCLC
- PD-L1 positive
- Have completed adjuvant chemotherapy at least 4 weeks and up to 12 weeks prior to randomization and must be adequately recovered from chemotherapy treatment
- ECOG Performance Status of 0 or 1
- Adequate hematologic and end-organ function
- For participants receiving therapeutic anticoagulation: stable anticoagulant regimen
- Negative for hepatitis B virus (HBV) or hepatitis C virus (HCV)
Exclusion Criteria
Exclusion Criteria: All Participants
- Any physical or cognitive condition that would prevent the participant from using the DHS
- Participants not proficient with any of the available DHS language translations or with psychiatric/neurologic disorders or any condition that may impact the participant's ability to use the DPM solution
- Currently participating in another interventional trial
- History of malignancy within 5 years prior to initiation of study treatment, with the exception of the cancer under investigation in this study and malignancies with a negligible risk of metastasis or death
Exclusion Criteria: Cohort A
- Concomitant anti-cancer therapy at the time of starting atezolizumab (IV) regimen on the index date which is not part of a locally approved combination therapy with atezolizumab
- Participants not receiving atezolizumab, but an atezolizumab biosimilar or non-comparable biologic
- Participants currently using another DPM or ePRO solution for symptom management and/or reporting
Exclusion Criteria: Cohort B
- Participants known to have a sensitizing mutation in the EGFR gene or an ALK fusion oncogene
- Uncontrolled tumor-related pain
- Uncontrolled pleural effusion, pericardial effusion, or ascites requiring recurrent drainage procedures (once monthly or more frequently)
- History of leptomeningeal disease
- Uncontrolled or symptomatic hypercalcemia
- Active or history of autoimmune disease or immune deficiency
- History of idiopathic pulmonary fibrosis, organizing pneumonia (e.g., bronchiolitis obliterans), drug-induced pneumonitis, or idiopathic pneumonitis, or evidence of active pneumonitis on screening chest computed tomography (CT) scan
- Active tuberculosis
- Significant cardiovascular disease
- Major surgical procedure, other than for diagnosis, within 4 weeks prior to initiation of study treatment, or anticipation of need for a major surgical procedure during the study
- Severe infection within 4 weeks prior to initiation of study treatment, including, but not limited to, hospitalization for complications of infection, bacteremia, or severe pneumonia, or any active infection that could impact participant safety
- Treatment with therapeutic oral or IV antibiotics within 2 weeks prior to initiation of study treatment
- Prior allogeneic stem cell or solid organ transplantation
- Treatment with a live, attenuated vaccine within 4 weeks prior to initiation of study treatment, or anticipation of need for such a vaccine during atezolizumab treatment or within 5 months after the final dose of atezolizumab
- Current treatment with anti-viral therapy for HBV
- Treatment with investigational therapy within 28 days prior to initiation of study treatment
- Prior treatment with CD137 agonists or immune checkpoint blockade therapies, including anti-CTLA-4, anti-PD-1, and anti-PD-L1 therapeutic antibodies
- Treatment with systemic immunostimulatory agents (including, but not limited to, interferon and IL-2) within 4 weeks or 5 drug elimination half-lives (whichever is longer) prior to initiation of study treatment
- Treatment with systemic immunosuppressive medication (including, but not limited to, corticosteroids, cyclophosphamide, azathioprine, methotrexate, thalidomide, and anti-tumor necrosis factor-α [TNF-α] agents) within 2 weeks prior to initiation of study treatment, or anticipation of need for systemic immunosuppressive medication during study treatment
- History of severe allergic anaphylactic reactions to chimeric or humanized antibodies or fusion proteins
- Known hypersensitivity to Chinese hamster ovary cell products or to any component of the atezolizumab formulation
- Pregnancy or breastfeeding
- Known allergy or hypersensitivity to hyaluronidase, bee or vespid venom, or any other ingredient in the formulation of rHuPH20
- Pathology (e.g., lower extremity edema, cellulitis, lymphatic disorder or prior surgery, preexisting pain syndrome, previous lymph node dissection, etc.) that could interfere with any protocol-specified outcome assessment
- Spinal cord compression not definitively treated with surgery and/or radiation, or previously diagnosed and treated spinal cord compression without evidence that disease has been clinically stable for ≥ 2 weeks prior to randomization
- Participants currently using another DPM or ePRO solution for symptom management and/or reporting
For the latest version of this information please go to www.forpatients.roche.com