ABEVMY™ CONCENTRATE FOR SOLUTION FOR INFUSION 25MG/ML

BIOCON BIOLOGICS LIMITED (INDIA)🇸🇬 Health Sciences Authority

Approval Date: Aug 29, 2022
Approval ID: c9a27ec9b45b0b6d
Company: BIOCON BIOLOGICS LIMITED (INDIA)
Type: Therapeutic

Approval Details

Approval Id: c9a27ec9b45b0b6d
Drug Name: ABEVMY™ CONCENTRATE FOR SOLUTION FOR INFUSION 25MG/ML
Product Name: ABEVMY™ CONCENTRATE FOR SOLUTION FOR INFUSION 25MG/ML
Approval Number: SIN16583P
Approval Date: 2022-08-29
Registrant: CEDAR PHARMACEUTICALS PTE. LTD.
Licence Holder: CEDAR PHARMACEUTICALS PTE. LTD.
Drug Type: Therapeutic
Forensic Classification: PRESCRIPTION ONLY MEDICINES
Dosage Form: INJECTION, SOLUTION, CONCENTRATE
Dosage: Dose and method of administration Substitution by any other biological medicinal product requires the consent of the prescribing physician. The safety and efficacy of alternating or switching between bevacizumab and products that are biosimilar but not deemed interchangeable to bevacizumab has not been established. Therefore, the benefit/risk of alternating or switching need to be carefully considered. Bevacizumab should be prepared by a healthcare professional using aseptic technique. Withdraw the volume of bevacizumab equivalent to the required dose per body weight and dilute in a total volume of 100 ml of sterile, pyrogen-free 0.9% sodium chloride. No incompatibilities between bevacizumab and polyvinyl chloride or polyolefin bags have been observed. Bevacizumab infusions should not be administered or mixed with dextrose or glucose solutions (see section Incompatibilities – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information). Do not administer as an intravenous push or bolus. The initial bevacizumab dose should be delivered over 90 minutes as an intravenous infusion. If the first infusion is well tolerated, the second infusion may be administered over 60 minutes. If the 60-minute infusion is well tolerated, all subsequent infusions may be administered over 30 minutes. The initial dose of bevacizumab should be administered following chemotherapy, all subsequent doses can be given before or after chemotherapy. Bevacizumab is not formulated for intravitreal use. (see section Special Warnings and Special Precautions for Use – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information) STANDARD DOSAGE Metastatic carcinoma of the colon or rectum (mCRC) The recommended dose of bevacizumab, administered as an intravenous infusion, is as follows: First-line treatment: 5 mg/kg of body weight given once every 2 weeks or 7.5 mg/kg of body weight given once every 3 weeks Second-line treatment: 10 mg/kg of body weight given every 2 weeks with FOLFOX-4. 5mg/kg every 2 weeks or 7.5mg/kg every 3 weeks when used in combination with fluoropyrimidine-irinotecan or fluoropyrimidine-oxaliplatin based chemotherapy regimen in patients who have progressed on a first-line bevacizumab -containing regimen (see section study ML18147 – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information). It is recommended that bevacizumab treatment be continued until progression of the underlying disease. Patients previously treated with bevacizumab can continue with bevacizumab treatment following first progression. Metastatic breast cancer (mBC) The recommended dose of bevacizumab, administered as an intravenous infusion, is as follows: In combination with paclitaxel: 10 mg/kg of body weight given once every 2 weeks. In combination with capecitabine: 15 mg/kg of body weight given once every 3 weeks. It is recommended that bevacizumab treatment be continued until progression of the underlying disease. Non-small cell lung cancer (NSCLC) First-line treatment of NSCLC in combination with platinum-based chemotherapy Bevacizumab is administered in addition to platinum-based chemotherapy for up to 6 cycles of treatment followed by bevacizumab as a single agent until disease progression. The recommended dose of bevacizumab is 15mg/kg of body weight given once every 3 weeks as an intravenous infusion. First-line treatment of NSCLC with EGFR activating mutations in combination with erlotinib The recommended dose of bevacizumab when used in addition to erlotinib is 15 mg/kg of body weight given once every 3 weeks as an intravenous infusion. It is recommended that the treatment with bevacizumab in addition to erlotinib is continued until disease progression. Please refer to the full prescribing information for erlotinib for patient selection and posology. Malignant Glioma (WHO Grade IV) – Glioblastoma The recommended dose of bevacizumab is 10 mg/kg of body weight given once every 2 weeks. It is recommended that bevacizumab treatment be continued until progression of the underlying disease. Advanced and/or metastatic Renal Cell Cancer (mRCC) The recommended dose of bevacizumab is 10 mg/kg of body weight given once every 2 weeks as an intravenous infusion. It is recommended that bevacizumab treatment be continued until progression of the underlying disease. Epithelial Ovarian, Fallopian Tube and Primary Peritoneal Cancer The recommended dose of bevacizumab administered as an intravenous infusion is as follows. Front-line treatment: 15 mg/kg of body weight given once every 3 weeks when administered in addition to carboplatin and paclitaxel for up to 6 cycles of treatment followed by continued use of bevacizumab as single agent until disease progression or for a maximum of 15 months or until unacceptable toxicity, whichever occurs earlier. Treatment of recurrent disease: Platinum sensitive: 15 mg/kg of body weight given once every 3 weeks when administered in combination with carboplatin and paclitaxel for 6 cycles and up to 8 cycles followed by continued use of bevacizumab as a single agent until disease progression. Alternatively, 15 mg/kg every 3 weeks when administrated in combination with carboplatin and gemcitabine for 6 cycles and up to 10 cycles followed by continued use of bevacizumab as single agent until disease progression. Platinum resistant: 10 mg/kg body weight given once every 2 weeks when administered in combination with one of the following agents <ul class="dash"> <li>paclitaxel, topotecan (given weekly) or pegylated liposomal doxorubicin (see section Study MO22224 for chemotherapy regimens – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information).</li> </ul> Alternatively, 15 mg/kg every 3 weeks when administered in combination with topotecan given on days 1 – 5, every 3 weeks (see Study MO22224 for chemotherapy regimen – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information). It is recommended that treatment be continued until disease progression. Cervical Cancer The recommended dose of bevacizumab is 15 mg/kg every 3 weeks as an intravenous infusion administered in combination with one of the following chemotherapy regimens: paclitaxel and cisplatin, or paclitaxel and topotecan (see study GOG-0240 for further details on the chemotherapy regimens – please refer to the Product Insert/Patient Information Leaflet published on HSA for the full drug information). It is recommended that bevacizumab treatment be continued until progression of the underlying disease.
Route Of Administration: INTRAVENOUS
Indication Info: Therapeutic indications Metastatic carcinoma of the colon or rectum(mCRC) Bevacizumab in combination with fluoropyrimidine-based chemotherapy is indicated for treatment of patients with metastatic carcinoma of the colon or rectum. Metastatic Breast Cancer (mBC) Bevacizumab in combination with paclitaxel is indicated for the treatment of patients who have not received chemotherapy for metastatic HER2-negative breast cancer. Bevacizumab in combination with capecitabine is indicated for first-line treatment of patients with HER2-negative metastatic breast cancer in whom treatment with other chemotherapy options including taxanes or anthracyclines is not considered appropriate. Patients who have received taxane and anthracycline-containing regimens in the adjuvant setting within the last 12 months should be excluded from treatment with bevacizumab in combination with capecitabine. The effectiveness of bevacizumab in metastatic breast cancer (mBC) is based on an improvement in progression-free survival. Currently, no data are available that demonstrate an improvement in disease-related symptoms or increased survival with bevacizumab in breast cancer. Non-Small Cell Lung Cancer (NSCLC) Bevacizumab, in combination with carboplatin and paclitaxel, is indicated for first-line treatment of patients with unresectable, locally advanced, recurrent or metastatic non-squamous, non-small cell lung cancer. Bevacizumab, in combination with erlotinib, is indicated for first-line treatment of patients with unresectable advanced, metastatic or recurrent non-squamous non-small cell lung cancer with Epidermal Growth Factor Receptor (EGFR) activating mutations. Malignant Glioma (WHO Grade IV) - Glioblastoma Bevacizumab, as a single agent is indicated for the treatment of patients with glioblastoma after relapse or disease progression following prior therapy. The effectiveness of bevacizumab in glioblastoma is based on an improvement in objective response rate. There are no data demonstrating an improvement in disease-related symptoms or increased survival with bevacizumab. Advanced and/or metastatic Renal Cell Cancer (mRCC) Bevacizumab in combination with interferon alfa-2a is indicated for first-line treatment of patients with advance and/or metastatic renal cell cancer. Epithelial Ovarian, Fallopian Tube and Primary Peritoneal Cancer Bevacizumab, in combination with carboplatin and paclitaxel is indicated for the front-line treatment of advanced (FIGO stages III B, III C and IV) epithelial ovarian, fallopian tube, or primary peritoneal cancer. Bevacizumab, in combination with carboplatin and gemcitabine or in combination with carboplatin and paclitaxel is indicated for the treatment of patients with recurrent, platinum-sensitive, epithelial ovarian, fallopian tube, or primary peritoneal cancer who have not received prior bevacizumab or other VEGF-targeted angiogenesis inhibitors. Bevacizumab in combination with paclitaxel, topotecan or pegylated liposomal doxorubicin is indicated for the treatment of patients with recurrent, platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal cancer who received no more than two prior chemotherapy regimens and who have not received prior therapy with bevacizumab or other VEGF inhibitors or VEGF receptor-targeted agents. Cervical Cancer Bevacizumab in combination with paclitaxel and cisplatin or paclitaxel and topotecan is indicated for the treatment of persistent, recurrent, or metastatic carcinoma of the cervix.
Contraindications: Contraindications Bevacizumab is contraindicated in: <ul class="dash"> <li>Patients with known hypersensitivity to any components of the product</li> <li>Patients with known hypersensitivity to Chinese hamster ovary cell products or other recombinant human or humanised antibodies.</li> <li>Pregnancy</li> </ul>
Atc Code: L01XC07
Atc Item Name: xl 01 xc 07
Pharma Manufacturer Name: ZUELLIG PHARMA PTE. LTD.
Company Detail Path: /organization/zuellig-pharma-pte-ltd

Active Ingredients

Bevacizumab

25 mg/ml

BEVACIZUMAB

25 MG/ML

Approved

Quick Info

Agency

HSA

Country

🇸🇬

Approval Date

Aug 29, 2022

Approval ID

c9a27ec9b45b0b6d

Type

Therapeutic

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