Product Description
1. Technical Specifications
| Attribute |
Details |
| Brand Name |
Tecentriq 1200 mg Injection |
| Generic Name |
Atezolizumab |
| Strength |
1200 mg per vial (concentrate for dilution) |
| Dosage Form |
Intravenous infusion (concentrate for solution for infusion) |
| Packaging Size |
Single-use vial (volume & vial size per manufacturer) |
| Packaging Type |
Glass vial with rubber stopper & flip-off seal |
| Medicine Type |
Immune checkpoint inhibitor Monoclonal antibody (anti-PD-L1) |
| Manufacturer |
Genentech / Roche (market dependent) |
| Distributed By |
Authorized oncology distributors / hospital pharmacies |
2. Product Description
Tecentriq contains atezolizumab, a humanized monoclonal antibody that binds programmed death-ligand 1 (PD-L1) on tumour cells and tumour-infiltrating immune cells. By blocking PD-L1 interaction with PD-1 and B7.1, it restores anti-tumour T-cell activity and enhances immune-mediated tumour cell killing. It is used alone or in combination with other agents for selected advanced cancers.
3. Product Highlights
| Attribute |
Details |
| Therapeutic Category |
Immune checkpoint inhibitor (anti-PD-L1 monoclonal antibody) |
| Application Area |
Multiple advanced malignancies (lung cancer, urothelial carcinoma, hepatocellular carcinoma, triple-negative breast cancer, extensive-stage small cell lung cancer, and others) use per approved indication and patient selection. |
| Mechanism of Action |
Binds PD-L1 prevents PD-L1/PD-1 interaction releases PD-1 mediated T-cell inhibition enhances anti-tumour immune response |
| Administration |
Intravenous infusion. Typical regimen: 1200 mg IV every 3 weeks (infuse over 60 minutes for first infusion; subsequent infusions may be given over 30 minutes if tolerated). Follow local label/protocol for combinations and alternative dosing schedules. |
| Storage Conditions |
Store refrigerated at 28 C; do not freeze; protect from light; handle as biological medicinal product. Use diluted infusion within manufacturer stability limits. |
4. Therapeutic Uses
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Non-Small Cell Lung Cancer (NSCLC): as monotherapy or in combination regimens for specific settings (dependent on histology, PD-L1 status and line of therapy).
-
Extensive-Stage Small Cell Lung Cancer (ES-SCLC): in combination with platinum-etoposide for first-line treatment (where approved).
-
Urothelial Carcinoma: for locally advanced or metastatic disease in selected settings (including maintenance use).
-
Hepatocellular Carcinoma (HCC): in combination with bevacizumab for selected patients.
-
Triple-Negative Breast Cancer (TNBC): in combination with chemotherapy for PD-L1positive advanced disease.
-
Other indications per local approval and label. Always confirm indication and patient selection (biomarkers, prior therapy) before use.
5. Side Effects
Common:
-
Fatigue, nausea, decreased appetite
-
Rash, pruritus
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Diarrhea
-
Infusion-related reactions (fever, chills, hypotension, dyspnea)
Immune-mediated (important / potentially severe):
-
Pneumonitis (new/worsening cough, dyspnea)
-
Colitis (diarrhea, abdominal pain)
-
Hepatitis (elevated AST/ALT, bilirubin)
-
Endocrinopathies (hypothyroidism, hyperthyroidism, hypophysitis adrenal insufficiency)
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Nephritis (renal dysfunction)
-
Dermatologic reactions (severe skin reactions are rare)
Serious / Rare:
6. Precautions & Monitoring
-
Baseline tests: CBC, liver function tests (AST/ALT, bilirubin), renal function, thyroid function (TSH free T4), and other tests as indicated. Screen for active infections per institutional practice.
-
Monitoring during therapy: Periodic LFTs, renal function, thyroid tests, and clinical assessment for signs/symptoms of immune-mediated toxicity. Monitor for infusion reactions during and after infusion.
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Management of immune-related AEs: Early recognition and prompt immunosuppressive therapy (corticosteroids) for moderate-to-severe events; hold or permanently discontinue therapy for severe or life-threatening toxicities per protocol.
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Vaccinations: Avoid live vaccines during treatment and until immune recovery.
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Pregnancy & Lactation: Use in pregnancy only if clearly needed; advise effective contraception during treatment and for a period after last dose. Avoid breastfeeding during therapy.
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Concomitant medications: Exercise caution with immunosuppressants; review agents that may mask immune-related AEs (e.g., systemic steroids) before starting therapy.
7. Administration & Practical Points
-
Reconstitute/dilute and administer according to product label and institutional pharmacy procedures.
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Premedication is not routinely required for most patients but may be used if prior infusion reactions occurred; follow institution guidance.
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Infusion rate: initial infusion 60 minutes; if tolerated, subsequent infusions may be given over 30 minutes. Do not administer as IV push/bolus.
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Use aseptic technique and in-line filter if recommended by manufacturer. Dispose of unused product and materials as per local regulations.
8. Handling & Storage
-
Store refrigerated (28 C); do not freeze or shake. Protect from light.
-
Prepare in a certified biological safety cabinet when required; observe cytotoxic/biologic handling precautions as per institutional policy.
-
Discard unused portion vials are single-use.
Advanced Immunotherapy for Cancer CareTecentriq 1200mg Injection represents a significant development in cancer treatment options. Its formulation targets specific pathways to help the bodys immune system fight certain cancers more effectively. As a prescription-only medication, it is intended for use under strict medical supervision, ensuring both safety and optimal benefit for adult patients.
Reliable Supply and DistributionOur distribution network provides Tecentriq 1200mg Injection to healthcare providers, exporters, suppliers, and wholesalers across India. Each batch is sourced with an emphasis on quality and reliability, ensuring that you receive authentic medicine handled under optimal storage conditions for maximum efficacy.
FAQs of Tecentriq 1200mg Injection:
Q: How is Tecentriq 1200mg Injection administered?
A: Tecentriq 1200mg Injection is given as an intravenous infusion by a qualified healthcare professional in a clinical setting. It should not be self-administered and must be administered as per your doctors instructions.
Q: What are the main benefits of using Tecentriq 1200mg Injection?
A: Tecentriq 1200mg Injection helps support the immune system in targeting and fighting certain types of cancer, offering an advanced option for improved clinical outcomes when standard therapies may not suffice.
Q: When should Tecentriq 1200mg Injection be used?
A: This injection should only be used when prescribed by a doctor, typically as part of a cancer treatment regimen for adults. The timing and dosage schedule are determined based on individual medical needs and cancer type.
Q: Where should Tecentriq 1200mg Injection be stored?
A: The injection must be stored in a cool and dry place, away from direct sunlight and moisture, to preserve its effectiveness. Always follow specific storage guidelines provided by the supplier or manufacturer.
Q: What is the process for obtaining Tecentriq 1200mg Injection in India?
A: Tecentriq is available through authorized distributors, exporters, suppliers, traders, and wholesalers in India. Healthcare institutions or pharmacies must place orders via these channels, ensuring all regulatory guidelines are observed.
Q: How should the correct dosage of Tecentriq 1200mg Injection be determined?
A: The appropriate dosage of Tecentriq is determined by the treating physician based on the patients condition, overall health, and specific treatment protocols. Never attempt to alter the dosage without medical consultation.
Q: What precautions must be taken during the usage of Tecentriq 1200mg Injection?
A: Ensure Tecentriq is administered only under medical supervision, adhere strictly to storage instructions, and immediately report any side effects to your healthcare provider. This approach helps to maximize efficacy and safety during treatment.