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| Name | Class |
|---|---|
| The Leukemia and Lymphoma Society | OTHER |
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The purpose of this study is to evaluate the safety and tolerability of AVL-292 as monotherapy in subjects with relapsed or refractory B cell non-Hodgkin lymphoma (B-NHL), chronic lymphocytic leukemia (CLL) or Waldenstrom's macroglobulinemia (WM).
Bruton's tyrosine kinase (Btk) is non-receptor tyrosine kinase with restricted cellular expression largely limited to B-lymphocytes, monocytes, and mast cells or basophils. Btk is a critical component of the B cell receptor (BCR) signaling network and is crucial for B cell development. Investigation has revealed that some B cell lymphomas and CLL depend on BCR signaling, suggesting that interruption of such signaling could be a promising therapeutic opportunity in B-NHL, CLL and WM.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| AVL-292 | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| AVL-292 | Drug | 125 mg to 625 mg orally, once a day, for 28 days (28 days equals 1 cycle). Number of cycles: until progression or unacceptable toxicity develops |
|
| Measure | Description | Time Frame |
|---|---|---|
| Safety, tolerability,and dose limiting toxicities will be determined using AEs,PE,ophthalmologic examinations,clinical laboratory tests,vital signs, ECGs and echocardiograms/MUGA scans. | with in the first 28 days after initiation of once daily oral dosing |
| Measure | Description | Time Frame |
|---|---|---|
| Establish recommended Phase 2 dose, after completing dose escalation in Part 1 and evaluating accumulated safety,PK,and PD data from the dose escalation phase (Part1) | After completion of observation for dose limiting toxicities in Part 1 of the study, the accumulated safety, PK, and PD data from Part 1 will be evaluated by the investigators and Sponsor to select a preliminary RP2D for administration to additional subjects to be enrolled into 1 of 3 independent and non-randomized diagnosis-specific expansion cohorts in Part 2 of the study |
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Inclusion Criteria:
Women and men ≥18 years of age
Body weight ≥50 kg.
Confirmed diagnosis of B cellNon-Hodgkin Lymphoma(according to World Health Organization [WHO] classification)including Chronic Lymphocytic Leukemia/Small cell Lymphocytic Leukemia (International Workshop),or Waldenstrom's Macroglobulinemia(Second International Workshop)
Have failed ≥1 previous treatment for B-NHL/CLL/WM, and have relapsed or refractory disease following last prior treatment.
Eastern Cooperative Oncology Group performance status of ≤ 2 and a life expectancy of at least 3 months.
Ability to swallow oral capsules without difficulty
Has recovered from adverse toxic effects of prior therapies
Meet the following clinical laboratory requirements:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Clearview Cancer Institute Oncology Specialties, P.C | Huntsville | Alabama | 35805 | United States | ||
| University of Arizona SPORE |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 27471698 | Background | Arnason JE, Brown JR. B cell receptor pathway in chronic lymphocytic leukemia: specific role of CC-292. Immunotargets Ther. 2014 Jan 24;3:29-38. doi: 10.2147/ITT.S37419. eCollection 2014. |
| Label | URL |
|---|---|
| Leukemia \& Lymphoma Society | View source |
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|
| Completion of Part 1 dose escalation phase of study |
| Evaluate the Pharmacokinetic parameters of AVL-292 | Serial blood sampling to enable PK characterization of AVL-292 will be performed for the Cycle1 Day 1 (C1D1) and Cycle 1Day 15 dose administrations. Additional samples will be obtained on C1D8 and C1D22.A non-compartmental model will be evaluated for all subjects. | First 28 days of dosing |
| Evaluate the Pharmacodynamics of AVL-292 by measurement of free Btk | The PD activity of AVL-292 will be studied with a quantitative assay using a covalent probe to directly assess free Btk in PBMC lysates. | First 28 days of dosing |
| Characterize preliminary anti-tumor efficacy of AVL-292 in relapsed and/or refractory B-NHL, CLL and WM | Efficacy response assessments will be formally assessed within 7 days preceding C2D1, C3D1, C5D1, C7D1, and EOT | After completion of 28 day cycle of treatment |
| Tucson |
| Arizona |
| 85719 |
| United States |
| University of California San Diego | La Jolla | California | 92093-0960 | United States |
| Mayo Clinic Jacksonville | Jacksonville | Florida | 32224 | United States |
| Northwestern University | Chicago | Illinois | 60611 | United States |
| Horizon Oncology Center | Lafayette | Indiana | 47905 | United States |
| Dana Farber Cancer Institute | Boston | Massachusetts | 02115 | United States |
| Mount Sinai School of Medicine and Mount Sinai Graduate School of Biological Sciences | New York | New York | 10029 | United States |
| University of Rochester Medical Center | Rochester | New York | 14642 | United States |
| Cleveland Clinic | Cleveland | Ohio | 44195 | United States |
| The University of Texas MD Anderson Cancer Center | Houston | Texas | 77030 | United States |
| University of Texas Health Sciences Center | San Antonio | Texas | 78229 | United States |
| US Oncology | The Woodlands | Texas | 77380 | United States |
| ID | Term |
|---|---|
| D016393 | Lymphoma, B-Cell |
| D015451 | Leukemia, Lymphocytic, Chronic, B-Cell |
| D008258 | Waldenstrom Macroglobulinemia |
| D008228 | Lymphoma, Non-Hodgkin |
| D008223 | Lymphoma |
| D007938 | Leukemia |
| ID | Term |
|---|---|
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
| D008232 | Lymphoproliferative Disorders |
| D008206 | Lymphatic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D007160 | Immunoproliferative Disorders |
| D007154 | Immune System Diseases |
| D015448 | Leukemia, B-Cell |
| D007945 | Leukemia, Lymphoid |
| D006402 | Hematologic Diseases |
| D002908 | Chronic Disease |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D054219 | Neoplasms, Plasma Cell |
| D020141 | Hemostatic Disorders |
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
| D010265 | Paraproteinemias |
| D001796 | Blood Protein Disorders |
| D006474 | Hemorrhagic Disorders |
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