Clinical trial · Interventional
Ofatumumab With Fludarabine and Cyclophosphamide in B-CLL Patients
An Open-labeled, Randomized, Two-dose, Parallel Group Trial of Ofatumumab, a Fully Human Monoclonal Anti-CD20 Antibody, in Combination With Fludarabine and Cyclophosphamide, in Patients With Previously Untreated B-cell CLL
NCT00410163CI-TRIAL-00013710BIFROSTcompletedPhase 2Results postedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
To investigate the safety and efficacy of two dose regimes of ofatumumab in combination with chemotherapy in previously untreated patients with B-CLL
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Leukaemia, Lymphocytic, Chronic | Leukemia | ONTOLOGY_EXACT | 0.85 |
Interventions
Interventions (4)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Cyclophosphamide | Drug | Cyclophosphamide | ALIAS |
| Fludarabine | Drug | Fludarabine | ALIAS |
| Ofatumumab 1000mg | Drug | Ofatumumab | ALIAS |
| Ofatumumab 500mg | Drug | Ofatumumab | ALIAS |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- Active Comparator 1
- description
- Each patient will receive a total of 6 infusions with ofatumumab every 4 weeks in combination with fludarabine and cyclophosphamide. The first infusion will be 300mg followed by 5 infusions of 500mg
- interventionNames
- Drug: Ofatumumab 500mg
- Drug: Fludarabine
- Drug: Cyclophosphamide
- type
- ACTIVE_COMPARATOR
- label
- Active Comparator 2
- description
- Each patient will receive a total of 6 monthly infusions with ofatumumab in combination with fludarabine and cyclophosphamide. The first infusion will be 300mg followed by 5 infusions of 1000mg
- interventionNames
- Drug: Ofatumumab 1000mg
- Drug: Fludarabine
- Drug: Cyclophosphamide
Primary outcomes (2)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Patients with active B-CLL and with an indication for treatment 2. Age ≥ 18 years 3. Following receipt of verbal and written information about the study, the patient must provide signed informed consent before any study related activity is carried out Exclusion Criteria: 1. Any previous treatment for B-CLL or any other treatments that can be considered active against B-CLL 2. Glucocorticoid unless given in doses ≤ 10 mg /day for other indications than B-CLL (e.g. asthma) 3. Known transformation of B-CLL 4. Known CNS involvement of B-CLL 5. Past or current malignancy, except for: 1. Cervical carcinoma Stage 1B or less 2. Non-invasive basal cell and squamous cell skin carcinoma 3. Malignant melanoma with a complete response of a duration of \> 10 years 4. Other cancer diagnoses with a complete response of a duration of \> 5 years 6. Chronic or current infectious disease requiring systemic treatment 7. Clinically significant cardiac disease 8. Significant concurrent, uncontrolled medical condition 9. History of significant cerebrovascular disease 10. Known HIV positive 11. Positive serology for hepatitis B, unless due to vaccination 12. Leukapheresis, except as a safety measure before chemotherapy 13. ECOG Performance Status of 3 or 4 14. Patients who at the time of inclusion are not expected to be able to complete the ofatumumab-FC regimen 15. Patients who have received treatment with any non-marketed drug substance or experimental therapy within 4 weeks prior to Visit 1 16. Current participation in any other interventional clinical study 17. Patients known or suspected of not being able to comply with a study protocol (e.g. due to alcoholism, drug dependency or psychological disorder) 18. Breast feeding women or women with a positive pregnancy test at Visit 1 19. Women of childbearing potential not willing to use adequate contraception for up to one year after last dose of ofatumumab. Adequate contraception is defined as hormonal birth control or intrauterine device. For patients in the USA the use of a double barrier method is also considered adequate.
References
Publications (2)
- BACKGROUNDWierda WG, Kipps TJ, Durig J, Griskevicius L, Stilgenbauer S, Mayer J, Smolej L, Hess G, Griniute R, Hernandez-Ilizaliturri FJ, Padmanabhan S, Gorczyca M, Chang CN, Chan G, Gupta I, Nielsen TG, Russell CA; 407 Study Investigators. Chemoimmunotherapy with O-FC in previously untreated patients with chronic lymphocytic leukemia. Blood. 2011 Jun 16;117(24):6450-8. doi: 10.1182/blood-2010-12-323980. Epub 2011 Apr 15. PMID 21498674
- DERIVEDJewell RC, Kipps TJ, Durig J, Griskevicius L, Stilgenbauer S, Smolej L, Mayer J, Hess G, Hernandez-Ilizaliturri FJ, Padmanabhan-Iyer S, Fang L, Goldstein N, Gorczyca M, Gupta I, Lisby S, Wierda WG; Hx-CD20-407 Study Investigators. Associations of ofatumumab exposure and treatment outcomes in patients with untreated CLL receiving chemoimmunotherapy. Leuk Lymphoma. 2017 Feb;58(2):348-356. doi: 10.1080/10428194.2016.1195497. Epub 2016 Jul 7. PMID 27389174