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Trial record 9 of 38 for:    Radioligand | Cancer

A Study to Evaluate Safety, Tolerability, Dosimetry, and Preliminary Efficacy of the HER2 Directed Radioligand CAM-H2 in Patients With Advanced/Metastatic HER2-Positive Breast, Gastric, and Gastro-Esophageal Junction (GEJ) Cancer

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ClinicalTrials.gov Identifier: NCT04467515
Recruitment Status : Recruiting
First Posted : July 13, 2020
Last Update Posted : May 7, 2021
Sponsor:
Information provided by (Responsible Party):
Precirix

Brief Summary:
This is a Phase 1/2 multi-center, open label, dose escalation and dose expansion study to evaluate safety, tolerability, dosimetry, pharmacodynamics (PD), and efficacy of the targeted radionuclide therapeutic CAM-H2 in patients with progressive, advanced/metastatic HER2-positive breast, gastric, and GEJ cancer with disease progression following anti-HER2 standard of care treatment. The study duration for each phase will be up to 18 months. The study is comprised of a Treatment Period, consisting of a maximum of 2 cycles (12 weeks per cycle) of study drug, and a 12-month Long-Term Follow-Up Period.

Condition or disease Intervention/treatment Phase
Advanced/Metastatic HER2-positive Breast, Gastric, Gastroesophageal Junction Cancer With Disease Progression Following Anti-HER2 Standard of Care Treatment Drug: CAM-H2 Phase 1 Phase 2

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 70 participants
Allocation: N/A
Intervention Model: Sequential Assignment
Intervention Model Description:

The dose escalation phase of the study will be an open label 3 + 3 design, where at least 3 patients are treated at each dose level.

In the dose expansion phase of the study, the patients will be given the recommended dose for Phase 2 (RDP2) determined in the dose escalation phase. Similar to the dose escalation phase, all patients will receive at least 1 cycle of CAM-H2.

Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Multi-Center Open Label Dose Escalation and Dose Expansion Study to Evaluate Safety, Tolerability, Dosimetry, and Preliminary Efficacy of the HER2 Directed Radioligand CAM-H2 in Patients With Advanced/Metastatic HER2-Positive Breast, Gastric, and GEJ Cancer
Actual Study Start Date : April 29, 2021
Estimated Primary Completion Date : January 17, 2025
Estimated Study Completion Date : January 17, 2025

Arm Intervention/treatment
Experimental: Dose Escalation and Expansion

The dose escalation phase of the study will be an open label 3 + 3 design, where at least 3 patients are treated at each dose level. Dose escalation will be done via increases of the nominal activity of CAM-H2 in cohorts of 3 to 6 patients.

In the dose expansion phase of the study, the patients will be given the RDP2 determined in the dose escalation phase. Similar to the dose escalation phase, all patients will receive at least 1 cycle of CAM-H2.

Drug: CAM-H2
All patients will receive at least 1 cycle of CAM-H2. Patients with CB may receive 2 cycles of CAM-H2, each cycle given as 2 IV administrations, 4 weeks apart.




Primary Outcome Measures :
  1. Proportion of patients achieving an objective response (CR or PR) with the use of CAM-H2 as measured by the RECIST version 1.1 [ Time Frame: 18 months ]
  2. Clinical benefit rate (CBR) of CAM-H2 using the equation CBR = CR + PR + SD, as measured by the RECIST version 1.1 [ Time Frame: 18 months ]

Secondary Outcome Measures :
  1. Progression Free Survival (PFS) for patients receiving CAM-H2 [ Time Frame: 18 months ]
  2. Duration of response (DoR) in patients receiving CAM-H2 [ Time Frame: 18 months ]
  3. CBR in brain in patients receiving CAM-H2, using RANO-BM [ Time Frame: 18 months ]
  4. PFS in patients with brain metastases receiving CAM-H2 [ Time Frame: 18 months ]
  5. Overall survival (OS) for patients receiving CAM-H2 [ Time Frame: 18 months ]
  6. Proportion of patients on CAM-H2 who develop anti-drug antibodies (ADAs) [ Time Frame: 18 months ]

Other Outcome Measures:
  1. Dosimetry - assessed by blood draws for blood and plasma gamma counts as well as by planar Whole body scans and SPECT/CT scans of the abdomen (kidney and liver) and of the target lesions [ Time Frame: 18 months ]
  2. Safety and Tolerability - Incidence and severity of treatment-emergent adverse events (TEAEs) [ Time Frame: 18 months ]
    Assessed by the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0

  3. Maximum tolerated dose (MTD) of CAM-H2 assessed by the number and type of DLTs as defined in the protocol that occur during the first cycle [ Time Frame: 18 months ]
  4. Dose-limiting toxicity (DLT) rate of CAM-H2 assessed by toxicities occurring within the first cycle [ Time Frame: 18 months ]
  5. RDP2 for CAM-H2 assessed by the number and type of DLTs as defined in the protocol that occur during the first cycle [ Time Frame: 18 months ]


Information from the National Library of Medicine

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

Inclusion Criteria:

  1. Informed consent form signed voluntarily before any study-related procedure is performed,indicating that the patient understands the purpose of, and procedures required for, the study and is willing to participate in the study.
  2. Males and females ≥ 18 years of age.
  3. Eastern Cooperative Oncology Group performance status of 0 to 1.
  4. HER2-positive locally advanced or metastatic breast cancer refractory to standard cancer treatment or HER2-positive locally advanced or metastatic gastric or GEJ cancer, refractory to standard cancer treatment.
  5. Patients should have a minimum of 1 measurable lesion on computed tomography (CT) or magnetic resonance imaging (MRI) as defined by RECIST version 1.1 within 4 weeks of the first dose of the study drug (Day 1). The lesion has to be a new lesion or progression of an existing lesion under the current therapy.
  6. Patients with brain metastases should have a minimum of 1 measurable lesion on MRI as defined by RANO-BM within 4 weeks of the first dose of the study drug (Day 1). The lesion has to be a new lesion or progression of an existing lesion under the current therapy.
  7. Any previous anti-HER2 treatment for advanced or metastatic disease is allowed. Patients with breast cancer should have had at least 2 previous systemic anticancer treatments for recurrent, locally advanced or metastatic cancer. Patients with gastric cancer or GEJ cancer should have had at least 1 previous anti-HER2 treatment.
  8. Life expectancy > 6 months.
  9. Adequate organ function, determined by the following laboratory tests performed within 21 days before screening:

    • Adequate kidney function with an estimated creatinine clearance of > 60 mL/min (Chronic Kidney Disease Epidemiology Collaboration formula).
    • Adequate hepatic function defined as an alanine aminotransferase (ALT) and aspartate aminotransferase (AST) < 2.5 the upper limit of normal (ULN), or < 5 ULN in patients with liver metastases, and total bilirubin < 2 x ULN.
  10. Baseline left ventricular ejection fraction ≥ 50% as measured by echocardiography or multigated acquisition scan.
  11. Absence of any psychological, family, sociological, or geographical circumstance that could potentially represent an obstacle to compliance with the study protocol and the follow-up schedule, as determined by the Investigator. These circumstances will be discussed with the patient before enrollment in the study.
  12. Female patients of childbearing potential (ie, ovulating, premenopausal, and not surgically sterile) must have a negative serum pregnancy test within 7 days prior to administration of study drug. Patients and their partners of childbearing potential must be willing to use 2 methods of contraception, 1 of which must be a barrier method, for the duration of the study and should be maintained until 6 months after study drug administration. Medically acceptable barrier methods include condom with spermicide or diaphragm with spermicide. Medically acceptable non-barrier contraceptive methods include intrauterine devices or hormonal contraceptives (oral, implant, injection, ring, or patch).

Exclusion Criteria:

  1. Presence of frank leptomeningeal disease as a unique central nervous system feature or in association with brain parenchymal measurable lesion(s).
  2. Symptomatic brain metastases. Note: Patients with asymptomatic treated and untreated brain metastases are eligible.
  3. Previous local therapy for brain metastases, such as neurosurgery, stereotactic radiotherapy, or whole brain radiotherapy, administered within 6 weeks prior to administration of CAM-H2.

    Note: Previous therapy for brain metastases administered at least 6 weeks prior to CAM-H2 administration will be permitted.

  4. For patients with brain metastases, any increase in corticosteroid dose during the week prior to enrollment.

    Note: Corticosteroid treatment in a stable dose or decreasing dose for at least 4 weeks prior to enrollment is allowed.

  5. Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection requiring parenteral antibiotics or psychiatric illness/social situations that would limit compliance with study requirements.
  6. Uncontrolled thyroid disease, defined as free triiodothyronine (T3) and free thyroxine (T4) > 3 x ULN at screening.
  7. Uncontrolled diabetes defined as a fasting serum glucose > 2 x ULN or glycated hemoglobin levels > 8.5% at screening.
  8. Gastrointestinal (GI) tract disease resulting in an inability to take oral medication, malabsorption syndrome, a requirement for intravenous (IV) alimentation, prior surgical procedures affecting absorption, or uncontrolled inflammatory GI disease (eg, Crohn's, ulcerative colitis).
  9. Current active hepatic or biliary disease (exception of patients with Gilbert's syndrome, asymptomatic gallstones, liver metastases, or stable chronic liver disease per Investigator assessment).
  10. Ongoing peripheral neuropathy of Grade > 2 according to the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.
  11. Severe and/or uncontrolled medical conditions or other conditions that could affect participation in the study such as:

    • Symptomatic congestive heart failure of New York Heart Association Class III or IV.
    • Unstable angina pectoris, symptomatic congestive heart failure, myocardial infarction within 6 months of start of study drug, serious uncontrolled cardiac arrhythmia, or any other clinically significant cardiac disease.
    • Liver disease, including cirrhosis and severe hepatic impairment.
  12. Active (acute or chronic) or uncontrolled severe infections.
  13. Known history of HIV, hepatitis B, or active hepatitis C virus at screening.
  14. Prior investigational anticancer therapy within 4 weeks prior to CAM-H2 administration.
  15. Patients who have had a major surgery or significant traumatic injury within 4 weeks of start of study drug, who have not recovered from side effects of any major surgery (defined as requiring general anesthesia), or have a major surgery planned during the course of the study.
  16. Other malignancies within the past 3 years except for adequately treated carcinoma of cervix or basal or squamous cell carcinomas of the skin or stage I uterine cancer.
  17. Radiation therapy for metastatic disease foci outside the brain, administered within 3 weeks before study enrollment.
  18. Known hypersensitivity to any of the study drugs, including inactive ingredients, including iodine allergy.
  19. History of significant comorbidities that, in the Investigator's judgement, may interfere with study conduct, response assessment, or informed consent.
  20. Unable or unwilling to complete the study procedures.
  21. Patients that cannot be hospitalized in a radionuclide therapy room.
  22. Patients that are unable to comply with thyroid protective pre-medication.
  23. Patients in whom bladder catheterization cannot be performed, or in patients who are unwilling to be catheterized if necessary.
  24. Patients with contraindications for undergoing MRI or CT, including for receiving contrast agents.
  25. Patient is the Investigator or sub-Investigator, research assistant, pharmacist, study coordinator, or other staff or relative thereof, who is directly involved in the conduct of the study.

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): NCT04467515


Locations
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Canada, Ontario
Princess Margaret Hospital Recruiting
Toronto, Ontario, Canada
Contact: Rebecca Wong    416 946 2983    Rebecca.Wong@rmp.uhn.ca   
Canada, Quebec
Hospital Notre Dame du CHUM Not yet recruiting
Montréal, Quebec, Canada
Contact: David Roberge    514 890 8254    david.roberge.chum@ssss.gouv.qc.ca   
McGill University Faculty of Medicine - Royal Victoria Hospital Not yet recruiting
Montréal, Quebec, Canada
Contact: Catalin Mihalcioiu    514 934 1934    catalin.mihalcioiu@muhc.mcgill.ca   
Sponsors and Collaborators
Precirix
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Precirix
ClinicalTrials.gov Identifier: NCT04467515    
Other Study ID Numbers: CAMH2_1001
First Posted: July 13, 2020    Key Record Dates
Last Update Posted: May 7, 2021
Last Verified: May 2021

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Disease Progression
Disease Attributes
Pathologic Processes