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Medexus Pharmaceuticals Inc MEDXF


Primary Symbol: T.MDP

Medexus Pharmaceuticals Inc. is a Canada-based specialty pharmaceutical company with a North American commercial platform. The Company has a portfolio of rare disease treatment solutions. Its focus is on the therapeutic areas of oncology, hematology, rheumatology, autoimmune diseases, allergy, and dermatology. It operates through two segments: Medexus Pharma Canada and Medexus Pharma USA. Its lead products are IXINITY (US), Rupall (Canada), Rasuvo (US) and Metoject (Canada), and Gleolan (US). IXINITY (US) is an intravenous recombinant factor IX therapeutic for use in patients with hemophilia B. Rupall (Canada) is a prescription allergy medication with a mode of action. Rasuvo (US) and Metoject (Canada) is a formulation of methotrexate designed to treat rheumatoid arthritis and other autoimmune diseases. Gleolan (US) is an optical imaging agent indicated in patients with glioma as an adjunct for the visualization of malignant tissue during surgery.


TSX:MDP - Post by User

Post by GoldenArmon Nov 03, 2021 9:08am
280 Views
Post# 34081279

What is Type A meeting

What is Type A meetingI got this from a Yahoo Finance. Basically good new but it takes time.

Type A Meetings

The FDA and the applicants of regulatory filings interact with each other during the review period regarding advice relating to the development and review of investigational new drugs and biologics. Four formal meetings occur during the PDUFA review period: Type A, Type B, Type B (end-of-phase) and Type C.

Type A meetings are necessary for proceeding with a stalled product development program or addressing an important related safety issue, according to the FDA.

Usually, the sponsor of a drug requests a Type A meeting to discuss clinical holds, seeking inputs as to how resolve the issue, or following the submission of a response to the hold — if the FDA and the sponsor deem that the development is stalled and a new path forward is to be discussed.

Before submitting a request, the sponsor has to contact the review division to discuss the appropriateness of the request.

The FDA schedules a Type A meeting with the sponsor within 30 days of receiving a request.

When a CRL is issued, companies usually file a resubmission. ...Type A meeting to discuss and gain clarity on the issues outlined in the CRL.

Path Forward

Following a Type A meeting, companies typically take the feedback from the meeting and use it to address the issues impeding drug development or approval.

medac will need to resubmit the NDA after it receives the minutes of the Type A meeting, which will be issued within 30 days of the meeting being held.

Once the resubmission is complete, the FDA will communicate its response within 30 days.

The resubmissions will be classified either as Class I or Class II resubmissions, with the decision coming through in two months for the former and six months for the latter.

Basically we are looking at 4 to 8 months before this gets through the highly political and run by idiot lawyers FDA. This is medac's problem.

In the mean time we can count on sales for Canada and Management needs to focus on generating sales from existing products and bring on new ones.
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