Ibrucent Capsule
Ibrutinib
140mg
Incepta Pharmaceuticals Ltd.
| Pack size | 12's Pack |
|---|---|
| Unite Price | 500.00 BDT |
Indications
Ibrucent Capsule is used for:
Ibrutinib, is a kinase inhibitor indicated for the treatment of patients with:
• Mantle cell lymphoma (MCL), who have received at least one prior therapy
Accelerated approval was granted for this indication based on overall response rate.
Continued approval for this indication may be contingent upon verification of clinical benefit in confirmatory trials.
• Chronic lymphocytic leukemia (CLL), who have received at least one prior therapy
• Chronic lymphocytic leukemia with 17p deletion
• Waldenström’s macroglobulinemia (WM)
Adult Dose
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma, Waldenström Macroglobulinemia
420 mg taken orally once daily (three 140 mg capsules once daily)
Mantle Cell Lymphoma
560 mg taken orally once daily (four 140 mg capsules once daily)
Hepatic impairment
Mild (Child Pugh class A): 140 mg PO qDay
Moderate-to-severe (Child Pugh Classes B and C): Avoid use
Child Dose
Safety and efficacy not established
Renal Dose
Administration
Administer once daily at approximately the same time each day. Capsules should be taken orally with a glass of water. The capsules should not be opened, broke, or chewed.
Contra Indications
Hypersensitivity. Concomitant use w/ St. John's wort-containing prep.
Precautions
• Hemorrhage: Should be monitored for bleeding
• Infections: Patients should be monitored for fever and infections and evaluated
promptly
• Cytopenias: Complete blood counts should be checked monthly
• Atrial Fibrillation: Patients should be monitored for atrial fibrillation
• Second Primary Malignancies: Other malignancies have occurred in patients, including skin cancers, and other carcinomas
• Tumor Lysis Syndrome (TLS): Patients should be monitored at risk for TLS (e.g. high tumor burden)
• Embryo-Fetal Toxicity: Can cause fetal harm. Women should be advised of the potential risk to a fetus and to avoid pregnancy while taking the drug
Pregnancy-Lactation
Pregnancy
Verify pregnancy status of females of reproductive potential prior to initiating ibrutinib
Advise females of reproductive potential to avoid pregnancy while taking ibrutinib and for up to 1 month after ending treatment; if this drug is used during pregnancy or if the patient becomes pregnant while taking this drug, inform of the potential hazard to a fetus
Advise men to avoid fathering a child while receiving ibrutinib, and for 1 month following the last dose of ibrutinib
Pregnancy testing
Conduct pregnancy testing in females of reproductive potential prior to initiating therapy
Lactation
No information regarding the presence of ibrutinib or its metabolites in human milk, the effects on the breastfed infant, or the effects on milk production
Interactions
Increased exposure w/ medicinal products that strongly or moderately inhibit CYP3A4. Avoid grapefruit & Seville oranges as these contain moderate inhibitors of CYP3A4. Decreased exposure w/ drugs increasing stomach pH (eg, PPIs). To minimize the potential GI tract interaction, oral narrow therapeutic range, P-gp or BCRP substrates eg, digoxin or methotrexate should be taken at least 6 hr before or after treatment.
Side Effects
Side effects of Ibrutinib :
>10% (MCL)
Increased serum creatinine, 1.5 x ULN (67%)
Platelets decreased, all grades (57%)
Diarrhea (51%)
Hemorrhage (48%)
Neutrophils decreased, all grades (47%)
Hemoglobin decreased, all grades (41%)
Fatigue (41%)
Musculoskeletal pain (37%)
Peripheral edema (35%)
URI infection (34%)
Nausea (31%)
Bruising (30%)
Neutropenia, grades 3 or 4 (29%)
Dyspnea (27%)
Constipation (25%)
Rash (25%)
Abdominal pain (24%)
Vomiting (23%)
Decreased appetite (221%)
Cough (19%)
Pyrexia (18%)
Stomatitis (17%)
Thrombocytopenia, grades 3 or 4 (17%)
UTI infection (14%)
Pneumonia (14%)
Skin infections (14%)
Asthenia (14%)
Muscle spasms (14%)
Dizziness (14%)
Sinusitis (13%)
Headache (13%)
Dehydration (12%)
Dyspepsia (11%)
Petechiae (11%)
Arthralgia (11%)
Epistaxis (11%)
>10% (CLL)
Platelets decreased, all grades (71%)
Diarrhea (63%)
Bruising (54%)
Neutrophils decreased, all grades (54%)
URT infection (48%)
Hemoglobin decreased, all grades (44%)
Fatigue (31%)
Rash (27%)
Musculoskeletal pain (27%)
Neutropenia, grades 3 or 4 (27%)
Pyrexia (25%)
Peripheral edema (23%)
Constipation (23%)
Arthralgia (23%)
Nausea (21%)
Stomatitis (21%)
Sinusitis (21%)
Dizziness (21%)
Vomiting (19%)
Cough (19%)
Muscle spasms (19%)
Headache (19%)
Skin infection (17%)
Petechiae (17%)
Decreased appetite (17%)
Hypertension (17%
Abdominal pain (15%)
Oropharyngeal pain (15%)
Dyspepsia (13%)
Asthenia (13%)
Chills (13%)
1-10% (MCL)
Anemia, grades 3 or 4 (9%)
Increased serum creatinine, 1.5-3 x ULN (9%)
Hemorrhage, grades 3 or 4 (5%)
Secondary primary malignancies (5%)
1-10% (CLL)
Pneumonia (10%)
UTI (10%)
Dyspnea (10%)
Peripheral neuropathy (10%)
Second malignancies (10%)
Anxiety (10%)
Insomnia (10%)
Thrombocytopenia, grades 3 or 4 (10%)
Mode of Action
Ibrutinib is a small-molecule inhibitor of BTK. Ibrutinib forms a covalent bond with a cysteine residue in the BTK active site, leading to inhibition of BTK enzymatic activity. BTK is a signaling molecule of the B-cell antigen receptor (BCR) and cytokine receptor pathways. BTK’s role in signaling through the B-cell surface receptors results in activation of pathways necessary for B-cell trafficking, chemotaxis, and adhesion. Nonclinical studies show that ibrutinib inhibits malignant B-cell proliferation and survival in vivo as well as cell migration and substrate adhesion in vitro.
Note
Ibrucent 140mg Capsule generic name is Ibrutinib. Ibrucent 140mg Capsule is manufactured by Incepta Pharmaceuticals Ltd.Ibrucent is availble in all over Bangladesh.
Mes BD drug index information on Ibrucent Capsule is not intended for diagnosis, medical advice or treatment; neither intended to be a substitute for the exercise of professional judgment.