RecruitingPhase 1NCT05131022

A Study of NX-5948 in Adults With Relapsed/Refractory B-cell Malignancies

A Phase 1, Dose Escalation, and Cohort Expansion Study Evaluating NX-5948, a Bruton's Tyrosine Kinase (BTK) Degrader, in Adults With Relapsed/Refractory B-cell Malignancies


Sponsor

Nurix Therapeutics, Inc.

Enrollment

572 participants

Start Date

Apr 13, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

This is a first-in-human Phase 1a/1b multicenter, open-label study designed to evaluate the safety and anti-cancer activity of NX-5948 in patients with advanced B-cell malignancies.


Eligibility

Min Age: 18 Years

Inclusion Criteria8

  • Age ≥18 years
  • Patients in Phase 1a (Dose Escalation) must have histologically confirmed R/R CLL, SLL, DLBCL (subgroups include Richter-transformed DLBCL, germinal center B-cell type, activated B-cell type, high-grade B-cell lymphoma with MYC and BCL-2 and/or BCL-6 rearrangements, high-grade B-cell lymphomas NOS), FL, MCL, MZL (subtypes include EMZL, MALT, NMZL, SMZL), WM, or PCNSL.
  • Patients in Phase 1a must meet the following:
  • o For non-PCNSL indications, received at least 2 prior lines of therapy and have no other available therapies known to provide clinical benefit. For PCNSL, received at least 1 prior line of therapy
  • Patients in Phase 1b (Safety and Cohort Expansion) must have 1 of the following histologically documented B-cell malignancies, must meet criteria for systemic treatment, and must have received prior therapies and/or molecular features based on details described for each cohort: CLL or SLL, DLBCL, MCL, FL, MZL, WM, or PCNSL/SCNSL.
  • Measurable disease per response criteria specific to the malignancy.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 (0-2 for patients with PCNSL and secondary CNS involvement).
  • Adequate organ and bone marrow function

Exclusion Criteria20

  • Known or suspected active prolymphocytic leukemia or Richter's transformation to Hodgkin's lymphoma prior to study enrollment
  • Prior treatment for the indication under study for anti-cancer intent that includes:
  • Radiotherapy within 2 weeks of planned start of study drug (excluding limited palliative radiation).
  • Prior systemic chemotherapy within 2 weeks of planned start of study drug.
  • Prior monoclonal antibody therapy within 4 weeks of planned start of study drug, except for patients enrolling in Cohort 16 (CLL with secondary wAIHA) where a 16-week washout period is required.
  • Prior small molecule therapy within 2 weeks or 5 half-lives (whichever is shorter) of planned start of study drug.
  • Autologous or allogeneic stem cell transplant within 100 days prior to planned start of study drug.
  • Chimeric antigen receptor (CAR) T-cell therapy within 100 days prior to start of study drug (within 60 days prior to start of study drug for Phase 1b).
  • Use of systemic corticosteroids outside of dosing limits described below and within 7 days prior to initiation of study treatment excepting those used as prophylaxis for radio diagnostic contrast. Patients with PCNSL/SCNSL: no greater than 40 mg/day prednisone, or equivalent. Patients with PCNSL/SCNSL using greater than 20 mg/day prednisone, or equivalent, must be clinically stable at that dose for 7 days. All other diagnoses: no greater than 20 mg/day prednisone or equivalent.
  • Use of systemic immunosuppressive drugs other than systemic corticosteroids for any medical condition within 60 days prior to first dose of study drug
  • Previously treated with a BTK degrader
  • Active, uncontrolled autoimmune hemolytic anemia (except for patients enrolling in Cohort 16) or active, uncontrolled autoimmune thrombocytopenia.
  • Patient has any of the following within 6 months of planned start of study drug:
  • Myocardial infarction, unstable angina, unstable symptomatic ischemic heart disease, or placement of a coronary arterial stent
  • Uncontrolled atrial fibrillation or other clinically significant arrhythmias, conduction abnormalities, or New York Heart Association (NYHA) class III or IV heart failure
  • Thromboembolic events (e.g., deep vein thrombosis, pulmonary embolism, or symptomatic cerebrovascular events), stroke, or intracranial hemorrhage
  • Any other significant cardiac condition (e.g., pericardial effusion, restrictive cardiomyopathy, severe untreated valvular stenosis, severe congenital heart disease, or persistent uncontrolled hypertension defined as systolic blood pressure \> 160 mmHg or diastolic blood pressure \> 100 mmHg despite optimal medical management)
  • Bleeding diathesis, or other known risk for acute blood loss.
  • History of Grade ≥ 2 hemorrhage within 28 days of planned start of study drug.
  • Active known concurrent malignancy or malignancy other than the one under study within the past 3 years. (Exceptions include, but are not limited to, patients with more recent history of basal or squamous cell skin cancer, superficial bladder cancer, or carcinoma in situ of the cervix or breast may enroll if they have undergone curative therapy and have no evidence of disease).

Interventions

DRUGNX-5948

Oral NX-5948


Locations(62)

City of Hope

Duarte, California, United States

University of California, San Francisco

San Francisco, California, United States

Colorado Blood Cancer Institute

Denver, Colorado, United States

Yale Cancer Center

New Haven, Connecticut, United States

University of Miami

Miami, Florida, United States

Florida Cancer Specialists

Sarasota, Florida, United States

Winship Cancer Institute of Emory University

Atlanta, Georgia, United States

Northwestern University

Chicago, Illinois, United States

National Institute of Health

Bethesda, Maryland, United States

Cayuga Medical Center

Ithaca, New York, United States

Memorial Sloan Kettering Cancer Center

New York, New York, United States

Duke University Medical Center

Durham, North Carolina, United States

University of Cincinnati Medical Center

Cincinnati, Ohio, United States

Cleveland Clinic

Cleveland, Ohio, United States

University of Pennsylvania, Abramson Cancer Center

Philadelphia, Pennsylvania, United States

MD Anderson Cancer Center

Houston, Texas, United States

Huntsman Cancer Institute

Salt Lake City, Utah, United States

Medical College of Wisconsin

Milwaukee, Wisconsin, United States

CHU Angers

Angers, France

Hôpital Avicenne

Bobigny, France

CHU de Nantes

Nantes, France

CHU Bordeaux

Pessac, France

CHU de Poitiers

Poitiers, France

Institut Curie-Site Saint-Cloud

Saint-Cloud, France

CHRU de Nancy

Vandœuvre-lès-Nancy, France

IRCCS - AOU di Bologna

Bologna, Italy

ASST Spedali Civili Brescia

Brescia, Italy

IRCCS Ospedale San Raffaele - Università Vita-Salute San Raffaele di Milano

Milan, Italy

IRCCS Ospedale San Raffaele

Milan, Italy

Fondazione Policlinico Universitario A. Gemelli IRCCS

Rome, Italy

University Medical Center Groningen

Groningen, Netherlands

Radboud University Medical Center

Nijmegen, Netherlands

Erasmus MC

Rotterdam, Netherlands

University Medical Center Utrecht

Utrecht, Netherlands

AidPort sp. Zo.o

Skórzewo, Greater Poland Voivodeship, Poland

Pratia MCM

Krakow, Lesser Poland Voivodeship, Poland

University Clinical Hostpital in Wroclaw

Wroclaw, Lower Silesian Voivodeship, Poland

Pratia MTZ

Warsaw, Masovian Voivodeship, Poland

National Institute of Oncology Warszawa

Warsaw, Masovian Voivodeship, Poland

Pratia Onkologia Katowice

Katowice, Silesian Voivodeship, Poland

Medical University of Lublin

Lublin, Poland

Hospital Universitari Vall d'Hebron

Barcelona, Spain

Hospital Clínic de Barcelona

Barcelona, Spain

Hospital Universitario de Cabuenes

Gijón, Spain

Hospital Ramón y Cajal

Madrid, Spain

Hospital Fundación Jimenez Díaz - START Madrid

Madrid, Spain

Universitätsspital Basel

Basel, Switzerland

Istituto Oncologico della Svizzera Italiana

Bellinzona, Switzerland

Inselspital - Universitatsklinik Bern

Bern, Switzerland

Hôpitaux Universitaires de Genève

Geneva, Switzerland

Kantonsspital St.Gallen

Sankt Gallen, Switzerland

University Hospital Zurich

Zurich, Switzerland

The Beatson WOS Cancer Center

Glasgow, Scotland, United Kingdom

St. James Hospital

Leeds, United Kingdom

Clatterbridge Cancer Center NHS Foundation Trust

Liverpool, United Kingdom

St. Bartholomew's Hospital, Barts NHS Trust

London, United Kingdom

Sarah Cannon Research Institute UK

London, United Kingdom

The Christie NHS Foundation Trust

Manchester, United Kingdom

Oxford University Hospitals NHS Foundation Trust

Oxford, United Kingdom

University Hospitals Plymouth NHS Trust

Plymouth, United Kingdom

University Hospital Southampton NHS Foundation Trust

Southampton, United Kingdom

Royal Marsden NHS Foundation Trust

Sutton, United Kingdom

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NCT05131022


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