Trial record 1 of 1 for:
CJDQ443A12101
Study of JDQ443 in Patients With Advanced Solid Tumors Harboring the KRAS G12C Mutation (KontRASt-01)
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| ClinicalTrials.gov Identifier: NCT04699188 |
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Recruitment Status :
Recruiting
First Posted : January 7, 2021
Last Update Posted : May 1, 2024
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Sponsor:
Novartis Pharmaceuticals
Information provided by (Responsible Party):
Novartis ( Novartis Pharmaceuticals )
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Brief Summary:
This is a phase Ib/II open label study. The escalation part will characterize the safety and tolerability of JDQ443 single agent and JDQ443 in combination with the other study treatments (TNO155 and tislelizumab) in advanced solid tumor patients. After the determination of the maximum tolerated dose / recommended dose for a particular treatment arm, dose expansion will assess the anti-tumor activity and further assess the safety, tolerability, and PK/PD of each regimen at the maximum tolerated dose / recommended dose or lower dose.
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| KRAS G12C Mutant Solid Tumors Carcinoma, Non-Small-Cell Lung Carcinoma, Colorectal Cancer of Lung Cancer of the Lung Lung Cancer Neoplasms, Lung Neoplasms, Pulmonary Pulmonary Cancer Pulmonary Neoplasms | Drug: JDQ443 Drug: TNO155 Biological: tislelizumab | Phase 1 Phase 2 |
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 475 participants |
| Allocation: | Non-Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Treatment |
| Official Title: | A Phase Ib/II Open-label, Multi-center Dose Escalation Study of JDQ443 in Patients With Advanced Solid Tumors Harboring the KRAS G12C Mutation |
| Actual Study Start Date : | February 24, 2021 |
| Estimated Primary Completion Date : | January 8, 2027 |
| Estimated Study Completion Date : | January 8, 2027 |
Resource links provided by the National Library of Medicine
MedlinePlus Genetics related topics:
Lung cancer
| Arm | Intervention/treatment |
|---|---|
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Experimental: Arm A
JDQ443
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Drug: JDQ443
KRAS G12C inhibitor |
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Experimental: Arm B
JDQ443 in combination with TNO155
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Drug: JDQ443
KRAS G12C inhibitor Drug: TNO155 SHP2 inhibitor |
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Experimental: Arm C
JDQ443 in combination with tislelizumab
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Drug: JDQ443
KRAS G12C inhibitor Biological: tislelizumab Anti PD1 antibody |
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Experimental: Arm D
JDQ443 in combination with TNO155 and tislelizumab
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Drug: JDQ443
KRAS G12C inhibitor Drug: TNO155 SHP2 inhibitor Biological: tislelizumab Anti PD1 antibody |
Primary Outcome Measures :
- Dose Escalation: Incidence and severity of dose limiting toxicities (DLTs) during the first cycle of monotherapy or combination treatment [ Time Frame: 21 days ]A dose-limiting toxicity (DLT) is defined as an adverse event or abnormal laboratory value assessed as having a suspected relationship to study drug, and unrelated to disease, disease progression, inter-current illness, or concomitant medications that occurs within the first cycle of treatment
- Dose Escalation: Incidence and severity of adverse events (AEs) and serious adverse events (SAEs) [ Time Frame: 24 months ]All information obtained on AE will be displayed by treatment group. Summary tables will include only AEs that started/worsened during the cycles of treatment (treatment-emergent AEs).
- Dose Escalation: Frequency of dose interruptions and reductions, by treatment [ Time Frame: 24 months ]Tolerability of study drug will be assessed by summarizing the number of and reason for dose delays and dose reductions.
- Dose Escalation: Dose intensity by treatment [ Time Frame: 24 months ]Dose intensity is defined as the ratio of actual cumulative dose received and actual duration of treatment.
- Dose Expansion: Overall response rate (ORR) per RECIST v1.1, by treatment [ Time Frame: 24 months ]Overall response rate is defined as the proportion of patients with a BOR of CR or PR according to RECIST 1.1, and will be summarized along with the corresponding 95% exact binomial confidence interval (CI). Applies to all groups except the brain metastasis group.
- Dose expansion: Overall intracranial response rate (OIRR) per mRANO-BM [ Time Frame: 24 months ]OIRR per mRANO-BM is defined as the proportion of participants with a best overall intracranial response (BOIR) of CR or PR according to mRANO-BM criteria, and will be summarized along with the corresponding 90% and 95% exact CI. Applies to brain metastasis group only.
- Dose expansion: Incidence and severity of AEs and SAEs [ Time Frame: 24 months ]All information obtained on AE will be displayed by treatment group. Summary tables will include only AEs that started/worsened during the cycles of treatment (treatment-emergent AEs). Applies to JDQ443 dose randomization group only.
- Dose expansion: frequency of dose interruptions and reductions, by treatment [ Time Frame: 24 months ]Tolerability of study drug will be assessed by summarizing the number of and reason for dose delays and dose reductions. Applies to JDQ443 dose randomization group only.
- Dose expansion: Dose intensity by treatment [ Time Frame: 24 months ]Dose intensity is defined as the ratio of actual cumulative dose received and actual duration of treatment. Applies to JDQ443 dose randomization group only
- Dose expansion: ORR per RECIST 1.1 of JDQ443 single agent in patients with non-small cell lung cancer (JDQ443 dose randomization group only) [ Time Frame: 24 months ]Overall response rate is defined as the proportion of patients with BOR of CR or PR according to RECIST 1.1, and will be summarized along with the corresponding 95% exact binomial confidence interval (CI). Applies to JDQ443 dose randomization group only
Secondary Outcome Measures :
- Dose Escalation and Expansion: ORR per RECIST v1.1 [ Time Frame: 24 months ]Overall response rate is defined as the proportion of patients with a BOR of CR or PR according to RECIST 1.1, and will be summarized along with the corresponding 95% exact binomial confidence interval (CI)
- Dose Escalation and Expansion: Best Overall Response (BOR) per RECIST v1.1 [ Time Frame: 24 months ]BOR is defined as the best overall confirmed response recorded from the start of the treatment until disease progression/recurrence.
- Dose Escalation and Expansion: Progression-free survival (PFS) per RECIST v1.1, Overall Survival (OS) [ Time Frame: 24 months ]Per RECIST 1.1, PFS is defined as the time from the date of start of treatment to the date of the first documented progression, or death. If patient has not had an event, PFS will be censored at the date of last adequate tumor assessment. PFS will be summarized using the Kaplan-Meier method, along with 95% CI
- Dose Escalation and Expansion: Duration of Response (DOR) per RECIST v1.1 [ Time Frame: 24 months ]Duration of response is defined as the time from the date of the first documented response (CR or PR), to the date of first documented progression, or death due any cause. Estimates will use Kaplan-Meier method, and median DOR and corresponding 95% CI will be presented.
- Dose Escalation and Expansion: Disease Control Rate (DCR) per RECIST v1.1 [ Time Frame: 24 months ]The disease control rate is calculated as the percentage of patients with advanced or metastatic cancer who have achieved complete response, partial response and stable disease. It will be summarized along with the corresponding 95% exact CI
- Dose Escalation and Expansion: Plasma or serum concentration vs time profiles (AUC) by treatment [ Time Frame: Up to 24 months ]AUC is defined as area under the plasma or serum concentration versus time curve after a dose of JDQ443, TNO155 and tislelizumab
- Dose Escalation and Expansion: Plasma concentration (Cmax) by treatment [ Time Frame: Up to 24 months ]Cmax is defined as the maximum observed plasma or serum drug concentration after single dose administration.
- Dose Escalation and Expansion: Time to achieve Cmax (Tmax) by treatment [ Time Frame: Up to 24 months ]Tmax is defined as the time to reach maximum plasma or serum drug concentration after single dose administration.
- Dose Escalation and Expansion: Antidrug antibody (ADA) incidence by treatment [ Time Frame: Up to 24 months ]To evaluate the immunogenicity of tislelizumab when dosed in combination with JDQ443 and/or TNO155 - only applicable to Arms C and D
- Dose Expansion: Dose intensity by treatment [ Time Frame: 24 months ]
- Dose Expansion: Frequency of dose interruptions and reductions, by treatment [ Time Frame: 24 months ]Tolerability of study drug will be assessed by summarizing the number of and reason for dose delays and dose reductions.
- Dose Expansion: Incidence and severity of dose limiting toxicities (DLTs) during the first cycle of monotherapy or combination treatment [ Time Frame: 21 days ]A dose-limiting toxicity (DLT) is defined as an adverse event or abnormal laboratory value assessed as having a suspected relationship to study drug, and unrelated to disease, disease progression, inter-current illness, or concomitant medications that occurs within the first cycle of treatment
- Dose Expansion: Incidence and severity of AEs and SAEs by treatment [ Time Frame: 24 months ]
- Dose expansion: Intracranial disease control rate (IDCR) per mRANO-BM [ Time Frame: 24 months ]IDCR is the proportion of participants with a confirmed BOIR of CR or PR or SD (or non-CR/non-PD) per mRANO-BM criteria. It will be summarized along with the corresponding 90% and 95% CI. Applies to the brain metastasis group only.
- Dose expansion: Best overall intracranial response (BOIR) per mRANO-BM [ Time Frame: 24 months ]BOIR is defined as the best overall confirmed response recorded from the start of the treatment until disease progression/recurrence per mRANO-BM, or until patient comes off study, whichever comes first. BOIR will be summarized along with the corresponding 95% exact CI. Applies to the brain metastasis group only.
- Dose expansion: Intracranial progression free survival (IPFS) per mRANO-BM [ Time Frame: 24 months ]IPFS is defined as the time from the date of start of treatment to the date of the first documented progression per mRANO-BM, or death due to any cause. If a patient has not had an event, IPFS will be censored at the date of last adequate tumor assessment. IPFS will be summarized using the Kaplan-Meier method. Median IPFS and IPFS probability at pre specified time-points will be presented along with 95% CI. Applies to the brain metastasis group only.
- Dose expansion: Duration of intracranial response (DOIR) per mRANO-BM [ Time Frame: 24 months ]DOIR is defined as the time from the date of first documented intracranial response of either CR or PR to the date of the first documented intracranial progression as per mRANO-BM criteria as assessed by central review or date of death due to underlying cause of cancer. DOIR will be summarized using the KM method if data permit. Median DOIR, with corresponding 95% CI. KM estimates for DOIR proportions at specific time points, along with 95% CI will also be provided. Applies to the brain metastasis group only.
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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:
- Adult patients with advanced (metastatic or unresectable) KRAS G12C mutant solid tumors who have received standard of care or are intolerant or ineligible to approved therapies
- ECOG Performance Status of 0 or 1
- At least one measurable lesion as defined by RECIST 1.1
- Prior treatment with a KRAS G12C inhibitor may be allowed for dose escalations of combinations and a subset of groups in dose expansion
Exclusion Criteria:
- Tumors harboring driver mutations that have approved targeted therapies, with the exception of KRAS G12C mutations
- Symptomatic brain metastases or known leptomeningeal disease. Patients with asymptomatic treated or untreated brain metastases may be eligible
- Clinically significant cardiac disease or risk factors at screening
- A medical condition that results in increased photosensitivity Other protocol-defined inclusion/exclusion criteria may apply.
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): NCT04699188
Contacts
| Contact: Novartis Pharmaceuticals | 1-888-669-6682 | novartis.email@novartis.com | |
| Contact: Novartis Pharmaceuticals | +41613241111 |
Locations
Show 44 study locations
Sponsors and Collaborators
Novartis Pharmaceuticals
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Novartis Pharmaceuticals |
| ClinicalTrials.gov Identifier: | NCT04699188 |
| Other Study ID Numbers: |
CJDQ443A12101 2020-004129-22 ( EudraCT Number ) |
| First Posted: | January 7, 2021 Key Record Dates |
| Last Update Posted: | May 1, 2024 |
| Last Verified: | April 2024 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | Yes |
| Plan Description: | Novartis is committed to sharing with qualified external researchers, access to patient-level data and supporting clinical documents from eligible studies. These requests are reviewed and approved by an independent review panel on the basis of scientific merit. All data provided is anonymized to respect the privacy of patients who have participated in the trial in line with applicable laws and regulations. This trial data availability is according to the criteria and process described on www.clinicalstudydatarequest.com |
| Studies a U.S. FDA-regulated Drug Product: | Yes |
| Studies a U.S. FDA-regulated Device Product: | No |
Keywords provided by Novartis ( Novartis Pharmaceuticals ):
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KRAS KRAS G12C Metastatic cancer Advanced cancer Enzyme inhibitor PD-1 |
SHP2 Targeted therapy Non-small-cell lung cancer colorectal cancer Molecular mechanisms of pharmacological action |
Additional relevant MeSH terms:
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Carcinoma Lung Neoplasms Neoplasms Carcinoma, Non-Small-Cell Lung Colorectal Neoplasms Neoplasms, Glandular and Epithelial Neoplasms by Histologic Type Respiratory Tract Neoplasms Thoracic Neoplasms Neoplasms by Site Lung Diseases Respiratory Tract Diseases Carcinoma, Bronchogenic |
Bronchial Neoplasms Intestinal Neoplasms Gastrointestinal Neoplasms Digestive System Neoplasms Digestive System Diseases Gastrointestinal Diseases Colonic Diseases Intestinal Diseases Rectal Diseases Tislelizumab Antineoplastic Agents, Immunological Antineoplastic Agents |