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IVVD INVIVYD INC US FDA Inspections 8-K Filing

NVVY

VVD

INVIVYD INC

(IVVD)

2024 8-K

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Summary

SPEAR Study Group

Product Expansion

Financial Statements

Product Expansion

Failure to Meet Listing Sta...

Director Appointment

Financial Results

Nasdaq Compliance

Q4 2024 Results

PEMGARDA Update

Director Resignation

Financial Results

Q3 2024 Results

Virology Data Release

Corporate Update

Clinical Trial Launch

PEMGARDA Update

COVID-19 Treatment Update

Financial Results

Management Changes

Annual Meeting of Stockholders

Financial Results and Corpo...

Departure of CEO and Appoin...

Financial Results Announcement

Departure of Director, Refi...

Other Special Situation

Sales Agreement

Clinical Trial Results

Financial Results Announcement

Earnings Report

Appointment of Director

Amendment to Certificate of...

Financial Results Announcement

Incentive Program Approval

Financial Results Announcement

Announcement of COVID-19 th...

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Invivyd, Inc. submitted a request for Emergency Use Authorization (EUA) to the U.S. FDA for VYD222 for the prevention of COVID-19 in immunocompromised individuals.

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INVIVYD INC

2024

8 K

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