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Columvi

Columvi

Manufacturer:

Genentech, Inc.
Concise Prescribing Info
Contents
Glofitamab

Information is sourced from publicly available references. The information is for educational purpose of healthcare professionals and we are not liable for any loss or damage.
Indications/Uses
Relapsed or refractory diffuse large B-cell lymphoma after 2 or more lines of systemic therapy in adults.
Dosage/Direction for Use
IV Pre-treatment w/ obinutuzumab: Obinutuzumab 1,000 mg on cycle 1 day 1 (7 days prior to Columvi initiation) as infusion at 50 mg/hr. May be escalated in 50 mg/hr increments every 30 mins to max of 400 mg/hr. Columvi dose step-up schedule: 2.5 mg on cycle 1 day 8 in 4 hr infusion duration. 10 mg on cycle 1 day 15 in 4 hr infusion duration. 30 mg on cycle 2 day 1 in 4 hr infusion duration. 30 mg on cycle 3-12 day 1 in 2 hr infusion duration. Each cycle is 21 days. Max treatment duration: 12 cycles or until disease progression or unmanageable toxicity occurs 1st.
Contraindications
Hypersensitivity.
MIMS Class
Targeted Cancer Therapy
ATC Classification
L01FX28 - glofitamab ; Belongs to the class of other monoclonal antibodies and antibody drug conjugates. Used in the treatment of cancer.
Presentation/Packing
Form
Columvi conc for soln for infusion 1 mg/mL
Packing/Price
1's
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