A multi-centre, open label, uncontrolled, Phase IIa clinical trial evaluating the safety and efficacy of NOX-A12 in combination with a background therapy of bendamustine and rituximab (BR) in previously treated patients with chronic lymphocytic leukemia (CLL) - NOX-A12 with a background therapy of bendamustine and rituximab in C

Phase 1

• Conditions: Relapsed chronic lymphocytic leukemia; MedDRA version: 14.1Level: PTClassification code 10008958Term: Chronic lymphocytic leukaemiaSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps); Therapeutic area: Diseases [C] - Blood and lymphatic diseases [C15]

• Registration Number: EUCTR2011-004672-11-IT
• Lead Sponsor: OXXON PHARMA AG

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2012-03-08
• Study Completion: 2017-04-24
• Last Update Posted: 21 December 2021

Recruitment & Eligibility

• Status: ot Recruiting
• Sex: All
• Target Recruitment: 28

Inclusion Criteria

1. Male of female, age =18 2. Diagnosis of B cell CLL 3. Relapsed, bendamustine-sensitive (response duration of at least 6 months as assessed by prior treating physician) or bendamustine-naive patients after at least one but not more than 3 prior treatment of their disease. 4. CLL in need of treatment (Binet C or A/B with active disease) according to the IWCLL guidelines 5. Subject must have measurable disease according to IWCLL guidelines 6. Pre-study WHO performance status of =2 and modified cumulative illness rating scale (CIRS) of less than 7 7. Signed and dated, written informed consent 8. Men and women of reproductive potential must agree to follow accepted birth control methods during treatment and for 3 months after completion of treatment 9. Acceptable liver function at screening: bilirubin =1.5 x ULN, AST and/or ALT =2.5 x ULN 10. Acceptable heamatological status: platelet count =75 x10 9/L, ANC > 0.75 x 10 9/L 11. Acceptable renal function: serum creatinine =1.5 ULN and/or creatinine clearance =50 ml/min (Cockcroft Gault formula) 12. No clinical significant abnormalities of liver volume, liver heamodynamics or elasticity, measured by abdominal ultrasound.
Are the trial subjects under 18? no
Number of subjects for this age range: 0
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 16
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 17

Exclusion Criteria

1. Relapse of B-cell CLL within 6 months after last chemotherapy 2. Subjects who have progressed to more aggressive B-cell cancers such as Richter's syndrome 3. CLL with either deletion of the short arm of chromosome 17 (17p-) or mutations associated with the loss of p53 4. The subject has a history of or is clinically suspicious of cancer related CNS disease 5. Hyperleukocytosis of > 50,000 WBC/µL 6. Autoimmune hemolytic anemia 7. Prior allogeneic stem cell transplant or patients who are considered to be candidates for allo SCT as assessed by their treating physician 8. Patient has a history of other active malignancies within three years prior to study entry, with the exception of: adequately treated in situ carcinoma of the cervix uteri; basal or squamous cell carcinoma of the skin; in situ carcinoma of the bladder; previous malignancy confirmed and surgically resected with curative intent. 9. The patient exhibits evidence of other clinically significant uncontrolled condition(s) including, but not limited to: uncontrolled systemic infection (viral, bacterial or fungal); diagnosis of fever and neutropenia within 1 week prior to study drug administration 10. Female subject is pregnant or breast feeding 11. Known infection with HIV, active Hepatitis B or Hepatitis C 12. The patient has a history of prior toxicity from bendamustine or rituximab that resulted in permanent discontinuation of treatments. 13. Treatment with other investigational drugs, or participation in another clinical trial within 30 days prior to study drug administration 14. Uncontrolled hypertension (defined as systolic blood pressure (BP) > 160 mmHg or diastolic BP >100mmHg) 15. Myocardial infarction or unstable angina within the past 6 months prior to study drug administration 16. Systemic illnesses or other severe concurrent disease including alcoholism which, in the judgment of the investigator, would make the patient inappropriate for entry into this study or interfere significantly with the proper assessment of safety and efficacy of the investigational treatment 17. Known or suspected of not being able to comply with the trial protocol 18. Having previously enrolled in this clinical trial

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified