Colorectal Cancer, Non Small Cell Lung Cancer, Pancreatic Ductal Adenocarcinoma, Triple Negative Breast Cancer
Conditions
Keywords
First-in-Human, Phase 1, Phase 2, Antibody, Monoclonal, IL1RAP, Safety, Tolerability, Cancer, Solid tumor, Malignant, Dose escalation, Dose expansion, CAN04, Immunoglobulin, Clinical Trial, Infusion, Antineoplastic, Anticancer
Brief summary
This study will evaluate the safety, tolerability, and preliminary antitumor activity of CAN04 both as a monotherapy and in combination with standard of care treatment in subjects with solid cancer tumors. Following completion of the first part, the dose escalation cohorts, and determination of maximum tolerated dose or recommended phase 2 dose (MTD/RP2D), safety and tolerability will be further evaluated in an expanded cohort of subjects with pancreatic or lung cancer, as monotherapy or in combination with the standard of care treatment and to identify the RP2D of CAN04 in combination with standard of care. In addition, early signs of efficacy during treatment with CAN04 will be investigated.
Detailed description
CAN04 is a first-in-class fully humanized and ADCC enhanced monoclonal antibody, targeting the Interleukin 1 Receptor Accessory Protein (IL1RAP). The CAN04 strategy is to attack the IL1RAP target molecule using an effective antibody-based cancer treatment. In preclinical (in vitro and in vivo) studies, CAN04 has shown two distinct mechanisms of action: 1. By blocking the intracellular signals from the IL1RAP target molecule, thereby impairing the cancer cells' ability to secrete tumor stimulating cytokines, in turn reducing tumor inflammation and tumor progression. 2. Through antibody dependent cellular cytotoxicity (ADCC) against IL1RAP expressing tumor cells where CAN04 stimulates natural killer (NK) cells to attack the tumor cells. The study is a combined phase 1/2a, open-label, dose-escalation followed by dose expansion, safety and tolerability clinical trial, in patients with relapsed or refractory solid tumors. It consists of two parts. In Part I (Dose Escalation - DE), the intention is to include patients with any of the four solid tumor types: Non-Small Cell Lung Cancer (NSCLC), Pancreatic Ductal Adenocarcinoma (PDAC), Triple Negative Breast Cancer (TNBC) or Colorectal Cancer (CRC). In this part of the study safety and tolerability will be documented and the MTD/ RP2D will be determined. Patients will stay on CAN04 treatment until disease progression, unacceptable toxicity, or discontinuation for any other reason. \[Completed December 2018\] In Part II (Expansion Cohort - EC), safety and tolerability will be further evaluated in an expanded cohort of subjects with PDAC or NSCLC to identify RP2D of CAN04 in combination with standard of care. In addition, early signs of efficacy during treatment with CAN04 will be investigated, as monotherapy or in combination with the standard of care. Patients will stay on treatment until disease progression, unacceptable toxicity, or discontinuation for any other reason. \[Enrollment to all arms completed\]
Interventions
BIOLOGICALCAN04
A fully humanized monoclonal immunoglobulin G1 (IgG1) antibody (hmAb) in aqueous solution administered by i.v. infusion.
DRUGCisplatin
Standard of care treatment
DRUGGemcitabine
Standard of care treatment
DRUGNab-paclitaxel
Standard of care treatment
DRUGCarboplatin
Standard of care treatment
DRUGPemetrexed
Standard of care treatment
Sponsors
Cantargia AB
Study design
Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
Part I of the study is designed to define the Maximum Tolerated Dose/ Recommended Phase 2 Dose (MTD/RP2D) of CAN04 in subjects with relapsed or refractory Non-Small Cell Lung Cancer (NSCLC), Pancreatic Ductal Adenocarcinoma (PDAC), Triple Negative Breast Cancer (TNBC) or Colorectal Cancer (CRC). \[Completed December 2018\] Part II consists of seven treatment arms and aims to establish the safety and tolerability of CAN04 as monotherapy and in combination with the standard of care in subjects with NSCLC or PDAC, as well as to investigate early signs of efficacy \[Enrollment to all arms completed\].
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Age ≥ 18 year. 2. Measurable disease in accordance to iRECIST by computed tomography (CT) or magnetic resonance imaging (MRI) scan, no more than 6 weeks prior to screening. 3. At least 4 weeks since the last dose of radiation therapy, immunotherapy, or surgery; at least 6 weeks for therapy which is known to have delayed toxicity; at least 4 weeks since treatment with biologic/targeted therapies. 4. Eastern Cooperative Oncology Group (ECOG) performance status ≤1. 5. Histologically or cytologically confirmed diagnosis of unresectable stage III or stage IV squamous or non-squamous NSCLC (applicable Part II, Combination - NSCLC (NCG) arm only). * Subjects must be eligible to receive first line standard chemotherapy regimen with cisplatin/gemcitabine or a second line standard chemotherapy regimen with cisplatin/gemcitabine after relapsing from first line with pembrolizumab monotherapy. * Subjects with actionable mutations (EGFR, ALK, ROS) can be enrolled if they have previously progressed to all approved standard of care targeted therapies and the next line of standard therapy is a platinum doublet. 6. Histologically or cytologically confirmed diagnosis of unresectable stage III or stage IV non-squamous NSCLC (applicable Part II, Combination - non-squamous NSCLC NCP arm only). * Subjects must be eligible to receive first line standard chemotherapy regimen with carboplatin/pemetrexed or a second line standard chemotherapy regimen with carboplatin/pemetrexed after relapsing from first line with pembrolizumab monotherapy. * Subjects with actionable mutations (EGFR, ALK, ROS) can be enrolled if they have previously progressed to all approved standard of care targeted therapies and the next line of standard therapy is a platinum doublet. 7. Newly diagnosed, treatment naїve, histologically confirmed, unresectable, locally advanced or metastatic (stage III or stage IV) PDAC (applicable Part II, Combination - PDAC arms only). * Subjects must be eligible to receive treatment with nab-paclitaxel and gemcitabine.
Exclusion criteria
1. Subjects receiving live vaccination, etanercept or other TNF-α inhibitors or any other investigational agents during or just prior to (within 28 days of first study drug administration) participation in this study. 2. Clinical evidence of an active metastatic second malignancy. 3. Subjects with a life expectancy \<12 weeks. 4. Uncontrolled or significant cardiovascular disease defined as New York Heart Association Classification III, or IV. 5. Immunocompromised subject currently receiving systemic therapy. 6. Other medical conditions that in the opinion of the investigator disqualify the subject for inclusion. 7. Applicable Part II, Combination - NSCLC (NCG and NCP) arms only * Prior lines of treatment with anti-cancer medication other than pembrolizumab administered as 1st line. * Known tumor EGFR mutation, unless contraindication to EGFR-directed therapy or if the subject has progressed to all approved anti-EGFR therapies. * Known tumor ALK rearrangements, unless contraindication to ALK-directed therapy or ALK-directed therapy not available or if the subject has progressed to all approved anti-EGFR therapies.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Incidence of Treatment-Emergent Adverse Events (Safety and Tolerability) | From the first dose until the last subject has completed their end of trial visit or the last enrolled subject has completed 6 months of treatment, whichever occurs first | The incidence of Grade 3 or higher adverse events (AEs) related to CAN04 administration and according to the National Cancer Institute - Common Terminology Criteria for Adverse Events (CTCAE, version 4.03). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Terminal half-life (t1/2) | 5 weeks | Terminal half-life of CAN04 |
| Clearance (CL) | 5 weeks | Plasma clearance of CAN04 |
| Apparent volume of distribution during the terminal phase (VZ) | 5 weeks | Apparent volume of distribution of CAN04 during the terminal phase |
| Maximum concentration (Cmax) | 5 weeks | Maximum plasma concentration of CAN04 |
| Anti-drug antibodies (ADA) against CAN04 | Through study completion, an average of 6 months | Immunogenicity of CAN04 after repeated administrations, assessed by ADA titers in serum. |
| Preliminary signs of efficacy as assessed by tumor response | One year | Tumor response (irRC Part I Part II Monotherapy arms; iRECIST Part II Combination arms) |
| Area under the curve from time 0 to infinity (AUC0-∞) | 5 weeks | Area under the plasma concentration curve from time 0 to infinity |
Countries
Austria, Belgium, Denmark, Estonia, Germany, Latvia, Lithuania, Netherlands, Norway, Spain, Sweden
Outcome results
None listed