Working…
COVID-19 is an emerging, rapidly evolving situation.
Get the latest public health information from CDC: https://www.coronavirus.gov.

Get the latest research information from NIH: https://www.nih.gov/coronavirus.
ClinicalTrials.gov
ClinicalTrials.gov Menu
Trial record 1 of 1 for:    MEGALiT
Previous Study | Return to List | Next Study

A MolEcularly Guided Anti-Cancer Drug Off-Label Trial (MEGALiT)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04185831
Recruitment Status : Recruiting
First Posted : December 4, 2019
Last Update Posted : October 28, 2020
Sponsor:
Information provided by (Responsible Party):
Peter Nygren, Uppsala University Hospital

Study Description
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information
Brief Summary:
This is a prospective, open-label, non-randomized combined basket- and umbrella trial divided in two parts; a limited feasibility-oriented part 1 including 154 patients and 3 treatment cohorts and part 2 that will include an expanded cohort of patients and treatment cohorts. The overall aims of the study are to test the feasibility, safety and efficacy of comprehensive genomic profiling on fresh tumor biopsies as a basis for treatment decision making and to compare two different sequencing, bioinformatics and decision-making platforms (part 1). Also to evaluate the efficacy and safety of off-label treatment with cancer drugs in patients selected based on genomic biomarker matching.

Condition or disease Intervention/treatment Phase
Solid Tumor Drug: Atezolizumab Drug: Everolimus Drug: Cobimetinib Phase 2

Detailed Description:
This is a prospective, open-label, non-randomized combined basket- and umbrella trial divided in two parts; a limited feasibility-oriented part 1 including 154 patients and 3 treatment cohorts (mutation/drug) and part 2 that will include an expanded cohort of patients and treatment cohorts. The overall aims of the study are to test the feasibility, safety and efficacy of comprehensive genomic profiling on fresh tumor biopsies as a basis for treatment decision making and to compare two different sequencing, bioinformatics and decision-making platforms (part 1). Also to evaluate the efficacy and safety of off-label treatment with cancer drugs in patients selected based on genomic biomarker matching.
Study Design
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 154 participants
Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Intervention Model Description: Combined umbrella and basket trial. Treatment selection based on mutation status.
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: MEGALiT - a Multicenter, Basket and Umbrella Explorative Trial on the Efficacy and Safety of Molecular Profile Selected Commercially Available Targeted Anti-cancer Drugs in Patients With Advanced Cancers Progressive on Standard Therapy
Actual Study Start Date : October 20, 2020
Estimated Primary Completion Date : December 2022
Estimated Study Completion Date : December 2022

Resource links provided by the National Library of Medicine


Arms and Interventions
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Arm Intervention/treatment
Experimental: NF1/MAP2K1
Cobimetinib, 60mg po daily. 28 day cycle; day 1-21 60mg daily, day 22-28 rest period.
 Drug: Cobimetinib
MEK inhibitor
Other Name: Cotellic
Experimental: MTOR/TSC1/TSC2
Everolimus, 10mg po daily.
 Drug: Everolimus
MTOR inhibitor
Other Name: Afinitor
Experimental: Mutation burden
Atezolizumab. 1200mg iv every 3 weeks.
 Drug: Atezolizumab
PD-L1 inhibitor
Other Name: Tecentriq


Outcome Measures
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Primary Outcome Measures :
  1. Objective Response Rate (ORR) and tumor control rate [Time Frame: From first dose up to 24 months] [ Time Frame: 1 year follow-up after LPFV ]
    The proportion of patients that have a best overall response of complete response (CR), partial response (PR) or stable disease ≥16 weeks, as assessed by RECIST 1.1 criteria


Secondary Outcome Measures :
  1. Additional measurements of treatment efficacy [ Time Frame: 1 year follow-up after LPFV ]
    Time to and duration of tumor response and stable disease, progression free survival, overall survival and progression free survival on study drug compared with that on the treatment preceding study drug treatment.

  2. Drug-related safety, evaluated according to the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) v4.03 [ Time Frame: 1 year follow-up after LPFV ]
    Incidence and severity of study drug related adverse events (AEs) and serious adverse events (SAEs). Include recording of changes in laboratory values, vital signs (body temperature, blood pressure, heart rate, respiratory rate), and assessment of physical, dermatological examinations graded according to the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) v4.03.

  3. Biopsy safety: NCI Common Terminology Criteria for Adverse Events 4.03 as grade 3 - 4 adverse event related to the procedure [ Time Frame: 1 year follow-up after LPFV ]
    Safety of core needle biopsy in advanced cancer scored according to NCI Common Terminology Criteria for Adverse Events 4.03 as grade 3 - 4 adverse event related to the procedure.

  4. Genomic analysis [ Time Frame: 1 year follow-up after LPFV ]
    Actionable target concordance between genomic analysis results from the Foundation Medicine platform F1CDx with that from the similar local analysis.

  5. Overall survival [ Time Frame: 1 year follow-up after LPFV ]
    Overall survival of patients starting treatment in accordance with 1 of the 4 groups of genomic markers compared with patients included in the trial but that do not start such treatment due to lack of appropriate marker.

  6. Feasibility of study design [ Time Frame: 1 year follow-up after LPFV ]
    Feasibility of comprehensive genomic testing of fresh tumor tissue for treatment decision, defined as the proportion of patients included with actionable genomic analysis within 4 weeks from inclusion


Eligibility Criteria
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Adult (age >18 years)
  2. Patients with histologically-proven, locally advanced or metastatic solid tumor (part 1; hematological malignancies also eligible in part 2) progressive while on last line established therapy considered available for the patient. For re-recruitment (part 2) patients must be progressive while on trial defined treatment or off-protocol treatment.
  3. Fresh tumor sampling by biopsy must be possible, except for patients with CNS malignancy who can be included based on molecular analysis of archived tumor material.
  4. ECOG performance status 0-2.

  5. Patients must have acceptable organ function as defined below:

    1. Absolute neutrophil count ≥ 1.5 x 10^9/L
    2. Hemoglobin > 90 g/L
    3. Platelets > 75 x 10^9/L
    4. Total bilirubin < 2 x ULN
    5. ASAT (SGOT) and ALAT (SGPT) < 2.5 x institutional ULN (or < 5 x ULN in patients with known hepatic metastases)
    6. Serum creatinine ≤ 1.5 × ULN or calculated or measured creatinine clearance ≥ 50 mL/min/1.73 m2
  6. Patients must have objectively measurable disease (by physical or radiographic examination).
  7. Ability to understand and the willingness to sign a written informed consent document.
  8. For orally administered drugs, the patient must be able to swallow and tolerate oral medication and must have no known malabsorption syndrome.
  9. Negative pregnancy test in women of childbearing potential (premenopausal or <12 months of amenorrhea post-menopause and who have not undergone surgical sterilization). Women of childbearing potential must use highly effective method of contraception, i.e. combined hormonal contraception, or progestogen-only hormonal contraception, or intrauterine device, or intrauterine hormone-releasing system, or bilateral tubal occlusion, or vasectomized partner, or sexual abstinence for the duration of participation in the study, and four months following completion of study therapy.
  10. Selected tumor types might have disease-specific inclusion criteria, defined by disease-specific study appendix.

Exclusion Criteria:

  1. Ongoing treatment-related toxicity > grade 2.
  2. Patients receiving any other anti-cancer therapy (cytotoxic, biologic, radiation, or hormonal other than for replacement) except for medications that are prescribed for supportive care but may potentially have an anti-cancer effect (e.g., megestrol acetate, bisphosphonates, somatostatin analogues and prednisone, or equivalent, >5 mg/d). These medications must have been started ≥ 1 week prior to the screening visit on this study. Radiotherapy to non-target lesions is allowed.
  3. Patients pregnant or nursing.
  4. Patients of childbearing potential and sexually active and not willing to use highly effective contraceptive.
  5. Patients with known active progressive CNS metastases. Patients with previously treated CNS metastases are eligible, provided that the patient has not experienced a seizure or had a clinically significant change in neurological status within the 3 months prior to inclusion. All patients with previously treated CNS metastases must be stable for at least 1 month after completion of treatment and off steroid treatment prior to inclusion.
  6. Some concomitant diseases qualified for exclusion as detailed in main protocol.
  7. Other serious underlying medical conditions, which, in the Investigator's judgment, could impair the ability of the patient to participate in the trial.
Contacts and Locations
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04185831


Contacts
Layout table for location contacts
Contact: Hannah Karlsson, PhD +46186171654 hannah.karlsson@akademiska.se

Locations
Layout table for location information
Sweden
Sahlgrenska University Hospital Recruiting
Gothenburg, Sweden
Contact: Lars Ny, MD, PhD       lars.ny@oncology.gu.se   
Principal Investigator: Lars Ny, MD, PhD         
Skane University Hospital Not yet recruiting
Lund, Sweden
Contact: Ana Carneiro, MD, PhD       ana.carneiro@med.lu.se   
Principal Investigator: Ana Carneiro, MD, PhD         
Uppsala University Hospital Recruiting
Uppsala, Sweden
Contact: Joakim Crona, MD, PhD       joakim.crona@medsci.uu.se   
Contact: Hannah Karlsson, PhD       hannah.karlsson@akademiska.se   
Principal Investigator: Joakim Crona, MD, PhD         
Sponsors and Collaborators
Uppsala University Hospital
Investigators
Layout table for investigator information
Principal Investigator: Peter Nygren, MD, PhD Uppsala University Hospital
Study Director: Peter Asplund, BSc Uppsala University Hospital
More Information
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information
Layout table for additonal information
Responsible Party: Peter Nygren, MD, PhD, professor in oncology, Uppsala University Hospital
ClinicalTrials.gov Identifier: NCT04185831    
Other Study ID Numbers: MEGALiT1901
First Posted: December 4, 2019    Key Record Dates
Last Update Posted: October 28, 2020
Last Verified: October 2020

Layout table for additional information
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Peter Nygren, Uppsala University Hospital:
mutation status
mutational burden
molecular profiling
precision medicine
Additional relevant MeSH terms:
Layout table for MeSH terms
Everolimus
Atezolizumab
Antineoplastic Agents
 Immunosuppressive Agents
Immunologic Factors
Physiological Effects of Drugs