Oncology Products
Select a product to view details
Bevagen®
Highlight
- First local Bevacizumab produce in Indonesia
- First line treatment in multi indications
- Affordable price
Indication
Metastatic Colorectal Cancer (mCRC), advanced/metastatic/recurrent Non-Small Cell Lung Cancer (NSCLC), locally recurrent or metastatic triple-negative Breast Cancer (mBC), epithelial ovarian, fallopian tube and primary peritoneal cancer, cervical cancer.
Specification:
- Form: Concentrate for solution for infusion
- Strength: 100 mg / 4 mL
- Pack: Box, 1 Vial @ 4 mL
- REG. BPOM: DKL2457901749A1
- Halal: ✓ Halal-certified
- Approvals: First local Bevacizumab in Indonesia
Bevagen® product range:
Bevagen® Bevacizumab 100mg/4mL
.
Brukinsa®
Highlight
- Based on clinical trials such as SEQUOIA and ALPINE, BRUKINSA demonstrates superior progression-free survival (PFS) compared to chemoimmunotherapy and first-generation BTK inhibitors.
- It exhibits a manageable safety profile in both elderly and younger adult patients, offering long-term efficacy, including in patients with genetic mutations such as Del 17p.
- Designed for high tolerability with minimal side effects.
Indication
Mantle Cell Lymphoma (MCL); Chronic Lymphocytic Leukemia (CLL) or Small Lymphocytic Lymphoma (SLL); Marginal Zone Lymphoma (MZL); Follicular Lymphoma (FL); Waldenstrom's Macroglobulinemia (WM).
Specification:
- Form: Capsules
- Strength: 80 mg
- Pack: Box, 120 Capsules
- REG. BPOM: DKI2468000201A1
- Approvals: NCCN Guidelines recommended
Brukinsa® product range:
Brukinsa® Zanubrutinib 80mg
.
Etapidi®
Highlight
- Etapidi demonstrated clinical benefit regardless of PD-L1 expression
- A promising PD-1 inhibitor approved in Indonesia
- Has been approved in over 40 countries, including the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA)
Indication
Non-Small Cell Lung Cancer (NSCLC), Esophageal Squamous Cell Carcinoma (ESCC), gastric cancer/gastroesophageal junction (GC/GEJ)
Specification:
- Form: Concentrate solution for IV infusion
- Strength: 100 mg / 10 mL
- Pack: Box, 1 Vial @ 10 mL
- REG. BPOM: DKI2468600149A1
- Approvals: US FDA · EMA · 40+ countries
Etapidi® product range:
Etapidi® Tislelizumab 100mg/10mL
.
Getana®
Highlight
- Firstline treatment for EGFR mutation NSCLC
- Affordable Price
- Listed in E-Catalogue
Indication
Gefitinib for locally advanced or metastatic non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) gene mutations.
Specification:
- Form: Film-coated tablets
- Strength: 250 mg
- Pack: Box, 3 blisters @ 10 film-coated tablets
- REG. BPOM: DKI2365600217A1
- E-Catalogue: Listed
Getana® product range:
Getana® Gefitinib 250mg
.
Hernera®
Highlight
- Irreversible pan-HER2 inhibitor for enhanced efficacy
- Additional recurrence risk reduction beyond trastuzumab-based therapy
- Convenient once-daily oral targeted therapy (Tyrosine Kinase Inhibitor - TKI)
Indication
As a single agent for the extended adjuvant treatment of adults with early-stage HER2-positive breast cancer following trastuzumab-based therapy; and in combination with capecitabine for the treatment of adults with advanced or metastatic HER2-positive breast cancer who have received two or more prior anti-HER2-based regimens in the metastatic setting.
Specification:
- Form: Film-coated tablets
- Strength: 40 mg
- Pack: Box, 1 Bottle @ 180 film-coated tablets
- REG. BPOM: DKI2570500117A1
Hernera® product range:
Hernera® Neratinib Maleate 40mg
.
Herzuma®
Highlight
- First line treatment in HER2-positive breast cancer
- Has been approved in over 100 countries
- Approved by the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA)
Indication
HER2-positive Early Breast Cancer (eBC), HER2-positive Metastatic Breast Cancer (mBC), and HER2-positive Metastatic Gastric Cancer (mGC).
Specification:
- Form: Powder for concentrate, IV infusion
- Strength: 440 mg
- Pack: 1 Vial
- BPOM: DKI2554100644A1
- Approvals: US FDA · EMA · 100+ countries
Herzuma® product range:
Herzuma® Trastuzumab 440mg
.
Truxima® Rituximab
Highlight
- The first rituximab biosimilar approved by the US FDA
- Has been approved in over 40 countries
- Approved by the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA)
- CD20-positive B-cell Non-Hodgkin's Lymphoma (NHL), CD20-positive B-cell Chronic Lymphocytic Leukemia (CLL).
Indication
Non-Hodgkin’s Lymphoma (NHL), Chronic Lymphocytic Leukaemia (CLL).
Specification:
- Form: Concentrate solution for IV infusion
- Strength: 100 mg / 10 mL · 500 mg / 50 mL
- Pack: 1 Vial
- REG. BPOM: DKI2454100549A1
- Halal: ✓ Halal-certified
- Approvals: US FDA · EMA · 40+ countries
Truxima® product range:
Truxima® Rituximab 100mg/10mL
Truxima® Rituximab 500mg/50mL
.
Zoledronic
Highlight
- Potent third-generation bisphosphonate
- High affinity to bone (long duration of action)
- Reduces risk of skeletal-related events (fractures, spinal compression)
- Effective in both oncology & metabolic bone diseases
- Convenient IV administration (once yearly /periodic dosing)
Indication
Bone metastases from solid tumors; hypercalcemia of malignancy; multiple myeloma; treatment and prevention of osteoporosis (postmenopausal & male); glucocorticoid-induced osteoporosis; Paget's disease of bone.
Specification:
- Form: Solution for IV injection
- Strength: 0.8 mg / mL
- Pack: 1 Vial @ 5 mL
- REG. BPOM: GKL2557902149A1
- BPJS: Listed
Zoledronic product range:
Zoledronic Acid Monohydrate 0,8mg/mL
.