for intravenous use Initial U.S. Approval: 2022
Kimmtrak (tebentafusp-tebn) is a medication used to treat unresectable or metastatic uveal melanoma, an aggressive cancer of the eye.
Facts about tebentafusp-tebn injection
Approval Date: 1/25/2022
Proprietary Name: Kimmtrak
Active Ingredient(s): tebentafusp-tebn
FDA-approved use: To treat unresectable or metastatic uveal melanoma
Dosage Form: Injection
Summary of FDA-approved use on approval date: Click Here
(see Drugs@FDA for complete indication)
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If you have a prescription from a Registered Medical Practitioner (RMP), IPN in Delhi can assist you in obtaining access to genuine medication. Our professional will provide you with a step-by-step guide on how to legally and safely import “tebentafusp-tebn injection” based on the information you provide.
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Query For tebentafusp-tebn injection
Approved accessible "tebentafusp-tebn injection"
Kimmtrak (tebentafusp-tebn) injection is the first therapy for metastatic or unresectable uveal melanoma, a rare cancer that develops in a part of the eye called the uvea.
Tebentafusp is indicated for HLA-A*02:01-positive adults with unresectable or metastatic uveal melanoma. Tebentafusp, sold under the brand name Kimmtrak, is an anti-cancer medication used to treat uveal melanoma (eye cancer). Tebentafusp is a bispecific gp100 peptide-HLA-directed CD3 T cell engager. Tebentafusp was approved for medical use in the United States in January 2022. The US Food and Drug Administration (FDA) considers it to be a first-in-class medication
How can 1 go about obtaining tebentafusp-tebn injection?
If tebentafusp-tebn injection are not yet approved or available in your area, you may request its price in India under a specific brand name through IPN. For assistance and guidance, you can contact us by providing complete details. Our pharmaceutical expert will help you find a suitable and practical solution to your query. To receive comprehensive support, please call us at +91 9891 296 838 (Mr. Tarun) / +91 9811 747 774 (Mr. Neeraj).
Kimmtrak (tebentafusp-tebn) injection for intravenous use Initial U.S. Approval: 2022
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