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RARE ULTRAGENYX PHARMACEUTICAL INC Product Launches 8-K Filing

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ULTRAGENYX PHARMACEUTICAL INC

(RARE)

2024 8-K

Royalty Agreement Signed

Patient Dosing Initiated

Positive DTX401 Results

FDA Application Start

Financial Statements

Product Expansion

Pre-Market Approval

Clinical Trials

Pre-Market Approval

Earnings Releases

Financial Results

FDA Application

Financial Results

FDA Designation

UX701 Study Update

Earnings Reports

FDA Meeting for Phase 3 Stu...

Annual Meeting and Election...

Public Offering

FDA Meeting for UX111 Gene ...

Phase 2/3 Orbit Study Results

Positive Phase 3 Results fo...

Financial Results Announcement

New Data from Phase 1/2 Stu...

Earnings Reports

Earnings Reports

Bylaws Amendment

Earnings Reports

Underwriting Agreement for ...

Pipeline Updates

Appointment Change

Financial Results Announcement

Annual Meeting Approval

Phase 2 Orbit study data an...

FDA Protocol Amendment

Earnings Report

Departure of Directors or C...

Financial Results Announcement

Earnings Reports

External Links:

Ultragenyx Pharmaceutical Inc. announced that the first patient has been dosed in its pivotal Phase 3 Aspire study for GTX-102, aimed at treating Angelman syndrome, which will involve about 120 children aged 4 to 17.

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ULTRAGENYX PHARMACEUTICAL INC

2024

8 K

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