Dose Optimization and Expansion Study of DFV890 in Adult Patients With Myeloid Diseases

Myeloid Diseases Clinical Trial

Official title:

A Phase 1b, Open Label, Multi-center, Dose Optimization and Dose Expansion Study to Assess the Safety and Efficacy of DFV890 in Adult Patients With Myeloid Diseases

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05552469
• Other study ID #: CDFV890G12101
• Status: Recruiting
• Phase: Phase 1
• Start date: May 8, 2023
• Est. completion date: June 30, 2026

Study information

• Verified date: March 2024
• Source: Novartis
• Contact: Novartis Pharmaceuticals
• Phone: 1-888-669-6682
• Email: novartis.email[@]novartis.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Study CDFV890G12101 is an open-label, phase 1b, multicenter study with a randomized two-dose optimization part, and a dose expansion part consisting of two groups evaluating DFV890 in patients with myeloid diseases. The purpose of this study is to assess the safety, tolerability, pharmacokinetics, pharmacodynamics, efficacy and recommended dose for single agent DFV890 in patients with lower risk (LR: very low, low or intermediate risk) myelodysplastic syndromes (LR MDS) and lower risk chronic myelomonocytic leukemia (LR CMML).

Description:

This research study is to find out if study treatment DFV890 is safe and tolerable, and can help patients who were diagnosed with a myeloid disease such as: very low, low or intermediate risk myelodysplastic syndromes (MDS) and very low, low or intermediate risk chronic myelomonocytic leukemia (CMML). The study seeks to determine the optimal dose of DFV890 that is safe and efficacious in patients with myeloid disease. The effectiveness and safety/tolerability of the study treatment is not yet confirmed in this disease setting.

Eligible patients meeting all study entry requirements will be required to provide a sample from their bone marrow at screening and at select study timepoints. All enrolled patients will be dosed for a minimum of twenty-four weeks (6 cycles of treatment) unless they experience side effects related to the study treatment requiring dose interruption/discontinuation, worsening of the disease, and/or if treatment is discontinued at the discretion of the investigator or the patient.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 80
• Est. completion date: June 30, 2026
• Est. primary completion date: June 30, 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Key Inclusion Criteria:

1. Patients must be = 18 years of age at the time of signing the informed consent form (ICF)

2. The Eastern Cooperative Oncology Group (ECOG) performance status (PS) = 2

3. Patient must be a candidate for serial bone marrow aspirate and/or biopsy according to the institutions guidelines and must be willing to undergo a bone marrow aspirate.

4. Patients must have one of the following for eligibility into the study:

1. In dose optimization and expansion: IPSS-R defined very low, low or intermediate risk Myelodysplastic Syndrome (LR MDS) who failed to respond to or did not tolerate ESAs or luspatercept or HMAs and patients with del 5q who failed to respond to or did not tolerate lenalidomide; or

2. In dose optimization and expansion: IPSS-R defined very low, low or intermediate risk Chronic Myelomonocytic Leukemia (LR CMML) who failed to respond to or did not tolerate hydroxyurea or HMAs.

Key Exclusion Criteria:

1. Systemic antineoplastic therapy (including cytotoxic chemotherapy, alpha-interferon, kinase inhibitors or other targeted small molecules, and toxin-immunoconjugates) or any experimental therapy within 28 days or 5 half-lives, whichever is longer, and recovered from the toxicities before the first dose of study treatment. For patients that received antibodies the washout period is 4 weeks prior to study treatment.

2. History of hypersensitivity to the study treatment or its excipients or to drugs of similar chemical classes.

3. Patients who have previously been treated with agents that have the same mechanism of action as DFV890 as defined in Table 6-8, list of prohibited medications (e.g., drugs targeting the NLRP3 inflammasome pathway and the IL-1 pathway (canakinumab and anakinra)).

4. Use of hematopoietic colony-stimulating growth factors (e.g., G-CSF, GM-CSF, M-CSF), thrombopoietin mimetics or erythroid stimulating agents anytime = 1 week (or 5 half lives, whichever is longer) prior to start of study treatment.

5. Patients receiving:

1. concomitant medications that are known to be modulators of cytochrome P450 enzymes CYP2C9 and/or CYP3A (specifically strong or moderate inducers of CYP2C9, strong inducers of CYP3A enzymes, strong inhibitors of CYP2C9 and/or strong or moderate dual inhibitors of CYP2C9/CYP3A); and

2. patients, who are poor CYP2C9 metabolizers receiving concomitant medications known to be strong or moderate inhibitors of CYP3A, whose concomitant medications cannot be discontinued or switched to a different medication within 5 half-lives or 1 week (whichever is longer) prior to start of study treatment and for duration of the study. See Section 6.8 and list of prohibited drugs in Appendix 8 for more details.

Other protocol-defined inclusion/exclusion criteria may apply.

Related Conditions & MeSH terms

• Myeloid Diseases

Intervention

Drug:
• DFV890
DFV890 Single Agent

Locations

Country	Name	City	State
France	Novartis Investigative Site	Grenoble
France	Novartis Investigative Site	Nantes Cedex 1
Germany	Novartis Investigative Site	Dresden
Germany	Novartis Investigative Site	Leipzig
Germany	Novartis Investigative Site	Velbert	North Rhine-Westphalia
Hong Kong	Novartis Investigative Site	Hong Kong
Italy	Novartis Investigative Site	Brescia	BS
Italy	Novartis Investigative Site	Rozzano	MI
Singapore	Novartis Investigative Site	Singapore
Singapore	Novartis Investigative Site	Singapore
Spain	Novartis Investigative Site	Madrid
Spain	Novartis Investigative Site	Madrid
United States	Sidney Kimmel CCC At JH	Baltimore	Maryland
United States	Dana Farber Cancer Institute .	Boston	Massachusetts
United States	Northwestern University	Chicago	Illinois
United States	Univ of TX MD Anderson Cancer Cntr	Houston	Texas
United States	Vanderbilt University Medical Ctr	Nashville	Tennessee
United States	Memorial Sloan Kettering Cancer Ctr	New York	New York
United States	Weill Cornell Medicine NY-Presb .	New York	New York
United States	Mayo Clinic - Rochester	Rochester	Minnesota
United States	Stanford Cancer Center Stanford Cancer Institute (2)	Stanford	California
United States	H Lee Moffitt Cancer Center and Research Institute	Tampa	Florida

Sponsors (1)

Lead Sponsor	Collaborator
Novartis Pharmaceuticals

Countries where clinical trial is conducted

United States,  France,  Germany,  Hong Kong,  Italy,  Singapore,  Spain, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incidence of Dose-limiting Toxicities (DLTs)	A dose-limiting toxicity (DLT) is defined as an adverse event or abnormal laboratory value assessed as clinically relevant, occurring during the DLT monitoring period following the first administration of study treatment.	28 days
Primary	Incidence and severity of Adverse Events (AEs) and Serious Adverse Events (SAEs)	Incidence and severity of AEs and SAEs by treatment group, including changes in vital signs, electrocardiograms (ECGs) and laboratory values qualifying and reported as AEs.	13 months
Primary	Incidence of dose interruptions, discontinuations and reductions	Number of patients with dose adjustments (interruptions, discontinuations and reductions) summarized by treatment group.	12 months
Secondary	Reduction in red blood cell (RBC) / platelet transfusions from baseline for transfusion-dependent (TD) patients	The number of red cell or platelet transfusions a patient receives over the course of study treatment will be compared to the patient's baseline transfusion requirements based on the transfusions received during the 16-weeks period prior to the start of study treatment.	Baseline, 12 months
Secondary	Percentage of patients developing transfusion independence (TI) for =8 weeks, =12 weeks, =16 weeks or =24 weeks for TD patients	Percentage of patients who develop red cell or platelet transfusion independence (defined as no red cell or platelet transfusions with a duration lasting for 8, 12, 16, or 24 weeks)	Baseline, 8 weeks, 12 weeks, 16 weeks and 24 weeks
Secondary	Best overall response (BOR) per 2006 IWG criteria for MDS and CMML	BOR is defined as the proportion of patients with best response recorded from the start of the treatment until disease progression/recurrence as per local investigator review and according to 2006 International Working Group (IWG) criteria	Baseline, 12 months
Secondary	Hematological improvement per 2006 IWG criteria for MDS and CMML	Number of participants with hematologic response will be based on erythroid response (HI-E), platelet response (HI-P), or neutrophil response (HI-N) as per local investigator review and according to 2006 IWG criteria	12 months
Secondary	Time to onset of transfusion independence	Time to onset of either red cell transfusion independence or platelet transfusion independence	12 months
Secondary	Duration of response (DOR)	DOR is defined as the duration from the first documented onset of any response to the date of progressive disease/relapse or death due to MDS/CMML	12 months
Secondary	Change from baseline in hemoglobin (Hb)	Hemoglobin levels over the course of the study will be compared to the patient's baseline to monitor for improvements in anemia	Baseline, 12 months
Secondary	Change from baseline in platelet count	Platelet count over the course of the study will be compared to the patient's baseline to monitor for improvements in thrombocytopenia	Baseline, 12 months
Secondary	Change from baseline in Absolute Neutrophil Count/White Blood Cells (ANC/WBC)	Ratio ANC/WBC over the course of the study will be compared to the patient's baseline to monitor for improvements in neutropenia	Baseline, 12 months
Secondary	Overall response rate (ORR)	ORR is the proportion of patients with a BOR of Complete Remission (CR) or Partial Remission (PR). Response is based on 2006 IWG criteria per local investigator review.	12 months
Secondary	Progression free survival (PFS)	PFS is defined as the time from the date of start of treatment to the date of the first documented progression, or death due to any cause. Response is based on 2006 IWG criteria per local investigator review.	12 months
Secondary	Time to progression (TTP)	TTP is defined as the time between date of first documented CR or PR to the date of first documented progression/relapse or death due to any cause, whichever occurs first. Response is based on 2006 IWG criteria per local investigator review.	12 months
Secondary	For CMML: reduction in spleen volume	Spleen volume over the course of the study will be compared to the patient's baseline	Baseline, 12 months
Secondary	For CMML: MPN-SAF total symptom score (TSS)	The Myeloproliferative Neoplasm Symptom Assessment Form (MPN-SAF) Total Symptom Score (TTS) will be used for the assessment of symptom burden at baseline and monitoring symptom status during the course of treatment. MPN-SAF TSS includes the assessment of 10 symptoms (fatigue, concentration, early satiety, inactivity, night sweats, itching, bone pain, abdominal discomfort, weight loss, and fevers). Severity of each symptom is rated on a 0 (absent/as good as it can be) to 10 (worst-imaginable/as bad as it can be) scale. MPN-SAF TSS has a possible range of scores of 0 to 100 with 100 representing the highest level of symptom severity.	Baseline, 12 months
Secondary	Maximum plasma concentration (Cmax) of DFV890	Pharmacokinetic parameters will be calculated based on DFV890 plasma concentrations by using non-compartmental method(s). Cmax is defined as the maximum (peak) observed concentration following a dose.	15 days
Secondary	Area under the plasma concentration-time curve from time zero to the last measurable concentration sampling time (AUClast) of DFV890	Pharmacokinetic parameters will be calculated based on DFV890 plasma concentrations by using non-compartmental method(s). AUClast is defined as the area under the plasma concentration-time curve from time zero to the last measurable concentration sampling time.	15 days