Ojemda (tovorafenib) Tablets and Oral Suspension

Ojemda, is an prescription medication. Its used to treat relapsed or refractory pediatric low-grade glioma.

NDA 218033
Drug Name: Ojemda
Active Ingredient: tovorafenib
Approval Date: 4/23/2024
FDA-approved use on approval date: To treat relapsed or refractory pediatric low-grade glioma
Company: Day One Biopharmaceuticals Inc.

Request Ojemda (tovorafenib) Communication – Important Information
If Ojemda (tovorafenib) is not available in your country, and you require assistance to get access this medication under “Named Patient Program (NPP)” treatment in the following city of India – Bengaluru, Delhi, Chennai, Hyderabad, Mumbai, Pune, Kolkata, Ahmedabad, Gurgaon, please send us a formal request for communication regarding this medication at urgent@cancermedicinesnetwork.com or call a customer support or WhatsApp your query

Please Note:
Ojemda (tovorafenib) is a prescription medication. A valid prescription from a licensed healthcare provider is required for any request.

Get In Touch

Get in touch with us at Verve Biscience, and one of our team will be on hand to help with any queries you may have.

The Verve Biscience is open
Monday to Saturday.
Business hours: 10.00 A.M to 06.00 P.M.

Contact Number:
M:+91-9910645395

Email ID:
info@cancermedicinesnetwork.com
rakeshkhanna.rk@gmail.com

Description

OJEMDA is a kinase inhibitor that is used to treat patients 6 months of age and older with relapsed or refractory pediatric low-grade glioma (LGG) harboring a BRAF fusion or rearrangement or BRAF V600 mutation.

Tovorafenib is indicated for the treatment of people six months of age and older with relapsed or refractory pediatric low-grade glioma harboring a BRAF fusion or rearrangement, or BRAF V600 mutation.

Tovorafenib was approved for medical use in the United States in April 2024, and is the first approval of a systemic therapy for the treatment of people with pediatric low-grade glioma with BRAF rearrangements, including fusions.

How to get access Ojemda (tovorafenib) for personal use ?

To get access to Ojemda (tovorafenib), you need a prescription from a doctor, as it is a prescription-only medication. Your prescription will be filled through a specialty pharmacy, which will handle insurance and coordinate delivery of the medication to you. Your doctor will also need to provide specific information for the prescription to be filled correctly.

However, patients in India can legally access it through the provision called the Named Patient Program (NPP). Ojemda (tovorafenib) prices may fluctuate over time because of market dynamics and regulatory changes. It can be imported for personal use under “Named Patient Program” treatment in multiple countries, including the Singapore, Kuala Lumpur (Malaysia), Bangkok (Thailand), Jakarta, Surabaya, Bandung (Indonesia), Manila, Cebu (Philippines), Ho Chi Minh City, Hanoi (Vietnam), Yangon (Myanmar), Phnom Penh (Cambodia), Vientiane (Laos), UAE, Saudi Arabia, Argentina, Brazil, UK, Hungary, Ireland, Latvia, Slovakia, Czech Republic, Belgium, Lithuania, Greece, Spain, Zimbabwe, Australia, and New Zealand.

To order or inquire about Ojemda (tovorafenib) international access, you can contact Verve Biosciences – a trusted pharmaceutical exporter, supplier, and distributor of anti-cancer and specialty medications.

📧 Email: urgent@cancermedicinesnetwork.com
📞 Call or WhatsApp: 9910645395 or 9910645395

Note: Availability may vary by country and is subject to regulatory approvals.

Delivered Countries

Serving over 65 countries worldwide with reliable pharmaceutical shipping across Asia-Pacific, Africa, Europe, the Middle East, North and South America.

North & South America: Canada, US, Mexico, Guatemala, El Salvador, Honduras, Costa Rica, Nicaragua, Panama, Cuba, Dominican Republic, Venezuela, Brazil, Bolivia, Chile, Peru, Ecuador Argentina, Columbia etc.
Europe (Germany, UK, France, Italy, Russia and Turkey etc.)
Asia-Pacific (China, Japan, Korea, India, Australia, Indonesia, Thailand, Philippines, Malaysia and Vietnam)
Middle East (Saudi Arabia, UAE, Egypt)
Africa: Ghana, Burkina, Togo, Benin, Nigeria, Nigeria, Cameroon, Sudan, Eritrea, Ethiopia, Somalia, Republic of Congo, (Democratic Republic of) Congo, Uganda, Kenya, Rwanda, Burundi, Tanzania, Zambia, Mozambique, Namibia, Botswana, Zimbabwe, South Africa.

About Healthcare Consultant

Rakesh brings an experience of 37 years in the pharmaceutical industry at various roles and responsibilities in Indian and US pharma MNCs. His areas of operations have been India and Southeast Asia, and he has been running a successful pharma business since 2010.

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Frequently Asked Questions (FAQs)

No. At present. This medicine is not approved by the Drug Controller General Of India (DCGI).

It is a prescription medicine. You should have a VALID and RECENT Prescription.

No, we do not sell rather we just FACILITATE the Procurement of this Medicine in India

Yes, We do. Since we facilitate the Procurement of Medicines directly from the International companies and that too with all Legal Documents like International Comp. Invoice, Air Way Bill (AWB) and Bill Of Entry (BOE), we Guarantee for it.

It would take you 12-17 Working Days as it requires Govt Approvals/Certificates and coordination with an International company.

A detailed answer to provide information about your business, build trust with potential customers, or help the visitor with a problem they may be encountering

A detailed answer to provide information about your business, build trust with potential customers, or help the visitor with a problem they may be encountering

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