A Phase 1/2 Study To Evaluate ASN002 In Relapsed/Refractory Lymphoma And Advanced Solid Tumors

Sponsor

Asana BioSciences (Industry)

Overall Status

Terminated

CT.gov ID

NCT02440685

Collaborator

(none)

Enrollment

Locations

Arms

Actual Duration (Months)

3.6

Patients Per Site

0.1

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This study is a dose escalation, and cohort expansion study in subjects with advanced cancer for which no standard therapy exists. Subjects must have received prior treatment for cancer that has not worked, or has stopped working.

Condition or Disease	Intervention/Treatment	Phase
Lymphoma, Large B-Cell, Diffuse Lymphoma, Mantle-Cell Lymphoma, Follicular Cancer Neoplasm Tumor Lymphoma, Malignant Lymphoma, B-cell Lymphoma, Non-Hodgkin B-Cell Chronic Lymphocytic Leukemia B-Cell Leukemia, Chronic B-Lymphocytic Leukemia, Chronic Chronic Lymphocytic Leukemia Leukemia, Lymphocytic, Chronic Leukemia, Lymphocytic, Chronic, B Cell Myelofibrosis Chronic Idiopathic Myelofibrosis Idiopathic Myelofibrosis Lymphoma, T Cell, Peripheral Peripheral T-Cell Lymphoma T-Cell Lymphoma, Peripheral	Drug: ASN002 Dose Escalation Drug: ASN002 RD	Phase 1/Phase 2

Detailed Description

The study will be conducted in two parts. Part A is a dose escalation study to determine a safe and tolerable dose of ASN002 for subjects with relapsed or refractory lymphoma, or advanced solid tumors. Part A will also characterize the pharmacokinetics and pharmacodynamics of ASN002 through blood sampling. Subjects in Part B will enroll subjects with four types of lymphoma Diffuse Large B-cell Lymphoma (DLBCL), Follicular Lymphoma (FL), Mantle Cell Lymphoma (MCL) and Peripheral T-cell lymphoma (PTCL). Additional groups of subjects with Myelofibrosis (MF) and Chronic Lymphocytic Leukemia (CLL) will be enrolled. Subjects will be treated with the highest safe and tolerable dose determined in Part A of the study to determine preliminary efficacy. Subjects may continue to receive ASN002 for up to 1 year in the absence of severe side effects or disease progression.

Study Design

Study Type:

Interventional

Actual Enrollment :

51 participants

Allocation:

Non-Randomized

Intervention Model:

Parallel Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

A Phase 1/2, Open-Label, Uncontrolled, Multiple Dose Escalation, Cohort Expansion Study To Evaluate The Safety, Tolerability, Pharmacokinetics And Preliminary Efficacy Of Asn002 In Relapsed/Refractory Lymphoma, Myelofibrosis, Chronic Lymphocytic Leukemia, And Advanced Solid Tumors

Actual Study Start Date :

May 1, 2015

Actual Primary Completion Date :

Jun 1, 2018

Actual Study Completion Date :

Jul 1, 2018

Arms and Interventions

Arm	Intervention/Treatment
Experimental: ASN002 Dose Escalation Multiple ascending doses of ASN002 will be administered to determine the maximum tolerated dose (MTD). Arm Closed	Drug: ASN002 Dose Escalation Multiple ascending doses of ASN002 assigned by cohort
Experimental: ASN002 Recommended dose (RD) - DLBCL ASN002 administered at the recommended dose in subjects with DLBCL. Arm Closed	Drug: ASN002 RD Recommended dose of ASN002 from Part A
Experimental: ASN002 RD - Mantle Cell Lymphoma ASN002 administered at the recommended dose in subjects with MCL. Arm Closed	Drug: ASN002 RD Recommended dose of ASN002 from Part A
Experimental: ASN002 RD - Follicular Lymphoma ASN002 administered at the recommended dose in subjects with FL.	Drug: ASN002 RD Recommended dose of ASN002 from Part A
Experimental: ASN002 RD - Peripheral T-cell Lymphoma ASN002 administered at the recommended dose in subjects with PTCL.	Drug: ASN002 RD Recommended dose of ASN002 from Part A
Experimental: ASN002 RD - Myelofibrosis ASN002 administered at the recommended dose in subjects with MF.	Drug: ASN002 RD Recommended dose of ASN002 from Part A
Experimental: ASN002 RD - Chronic Lymphocytic Leukemia ASN002 administered at the recommended dose in subjects with CLL.	Drug: ASN002 RD Recommended dose of ASN002 from Part A

Outcome Measures

Primary Outcome Measures

Part A: Determine the maximum tolerated dose (MTD) of ASN002 [First 28 days]
The MTD will be determined by evaluating the number of subjects with treatment related dose limiting toxicity. This is the primary endpoint of Part A
Part B: evaluate the overall response rate (number of Complete Responses + Partial Responses) in subjects receiving ASN002 for the treatment of lymphoma, MF and CLL. [First 6 months]
Change from baseline in the severity of disease, This is the primary endpoint for Part B.

Secondary Outcome Measures

Calculate the pharmacokinetic area under the plasma concentration (AUC) of ASN002 [First 29 days]
Calculate the amount of ASN002 in the bloodstream
Calculate the maximum plasma concentration (Cmax) at steady state. [First 29 days]
Calculate the maximum amount of ASN002 in the bloodstream
Calculate the terminal elimination rate (T 1/2). [First 29 days]
Calculate how fast ASN002 leaves the body

Other Outcome Measures

To evaluate the change from baseline in the intensity of Phospho-STAT3 protein found in the blood of patients with lymphoma. [First 29 days]
Evaluate the effect of ASN002 on tumor biomarkers
To evaluate the change from baseline in the intensity of Phospho-S6 protein found in the blood of patients with lymphoma. [First 29 days]
Evaluate the effect of ASN002 on biomarkers
To evaluate the change from baseline in the intensity of Phospho-spleen tyrosine kinase (SYK) 525/526 protein found in the blood of patients with lymphoma.. [First 29 days]
Evaluate the effect of ASN002 on biomarkers
To evaluate the change from baseline in the intensity of Phospho-extracellular signal-regulated kinases (ERK) protein found in the blood of patients with lymphoma. [First 29 days]
Evaluate the effect of ASN002 on biomarkers
The number of patients who show a decrease from baseline in a serum panel of biomarkers of inflammation [First 29 days]
Evaluate the effect of ASN002 on biomarkers

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Written informed consent obtained prior to any study-related procedure being performed;
Male or female subjects at least 18 years of age at the time of consent;
Eastern Cooperative Oncology Group (ECOG) Performance Status 0-2;
Recovered from the reversible effects of prior antineoplastic therapy (with the exception of alopecia and Grade 1 neuropathy).
Screening blood counts of the following: Absolute neutrophil count ≥ 1000/μL, Platelets ≥ 75,000/μL, Hemoglobin ≥ 8 g/dL (with transfusion support);
Screening chemistry values of the following: Alanine aminotransferase (ALT) and aspartate transaminase (AST) ≤ 3.0 × upper limit of the normal (ULN), total bilirubin ≤ 1.5 × ULN, Creatinine ≤ 1.5 × ULN;
At screening, life expectancy of at least 3 months;
Subject is willing and able to comply with all protocol required visits and assessments;
Male and female subjects of child-bearing potential must agree to use medically acceptable methods of birth control throughout the study and for thirty (30) days after the last dose of study medication.
(Part A only) Histologically or cytologically confirmed metastatic and/or advanced solid tumors or lymphomas for which no standard therapy exists, or who are not eligible for standard treatment. Subjects must have received at least one prior therapy for their malignancy;
(Part B only) Histologically confirmed DLBCL/MCL/FL/PTCL/MF/CLL on the basis of excisional lymph node or extranodal tissue biopsy; diagnosis of relapsed/refractory disease defined as 1) recurrence of disease after a Complete Response (CR), or 2) Partial Response (PR), Stable Disease (SD) at completion of treatment regimen preceding entry into study, subjects must not be candidates for standard therapy, subjects who have not received Stem Cell Translplant (SCT) must be ineligible to receive SCT.

Exclusion Criteria

Have received prior chemotherapy regimens within 4 weeks of Day 1;
Have received prior treatment with monoclonal antibodies within 6 weeks of first dose of Day 1;
Have had major surgery within 30 days prior to the start of Day 1;
Received any investigational treatment within 4 weeks prior to the start of study medication;
Have had an infection requiring the use of parenteral antibiotics within 14 days prior to the start of Day 1;
Have known central nervous system metastasis or Central Nervous System lymphoma;
Is receiving high dose corticosteroids (>10 mg prednisone daily or equivalent);
Has known bleeding diathesis that would be a safety risk;
Has a history of other malignancy within the 3 years prior to screening, except adequately treated basal cell or squamous cell carcinoma of the skin, or carcinoma in-situ;
Has difficulty swallowing medications, or known history of malabsorption syndrome;
Has a serious concurrent medical condition, such as: congestive heart failure New York Heart Association (NYHA) class III or IV or uncontrolled hypertension at screening, 12-Lead electrocardiogram (ECG) abnormalities considered by the investigator to be clinically significant including myocardial infarction, angioplasty, or cardiac stent placement within the last 6 months, HIV infection, known Hepatitis B or C infection. Subjects at high risk for Hepatitis B or C infection should have serology testing to rule out infection, a medical condition requiring the therapeutic use of anticoagulants.
Known hypersensitivity to ASN002 or its excipients;
Prior participation, i.e., receipt of study medication, in this study;
Any condition that, in the opinion of the investigator, would impair the subject's ability to comply with study procedures;
Female subjects that are pregnant or lactating.
Part B only: Prior treatment with SYK or Janus Kinase (JAK) inhibitors, except MF subjects.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Arizona Oncology	Tempe	Arizona	United States	85206
2	University of California, San Francisco	San Francisco	California	United States	94122
3	Winship Cancer Institute - Emory	Atlanta	Georgia	United States	30322
4	University of Michigan	Ann Arbor	Michigan	United States	48109
5	START - Midwest	Grand Rapids	Michigan	United States	49503
6	University of Mississippi Medical Center	Jackson	Mississippi	United States	39216
7	Gabrail Cancer Center	Canton	Ohio	United States	44718
8	Oregon Health & Science University	Portland	Oregon	United States	97239
9	Fox Chase Cancer Center	Philadelphia	Pennsylvania	United States	19111
10	MD Anderson Cancer Center	Houston	Texas	United States	77030
11	South Texas Accelerated Research Therapeutics	San Antonio	Texas	United States	78229
12	Virginia Cancer Specialists	Fairfax	Virginia	United States	22031
13	Hospital Universitario Austral	Buenos Aires	Derqui, Pilar	Argentina	1629
14	Instituto Alexander Fleming	Ciudad Autonoma de Buenos Aires		Argentina	1426