Invivyd to Present Data at 2024 American Society of Clinical Oncology (ASCO) Annual Meeting and 2024 American Transplant Congress (ATC)
29 Maggio 2024 - 1:00PM
Invivyd, Inc. (Nasdaq: IVVD), a biopharmaceutical company devoted
to delivering protection from serious viral infectious diseases,
today announced that it will present preliminary, subset analyses
from the CANOPY Phase 3 clinical trial of VYD222 (pemivibart) for
pre-exposure prophylaxis of COVID-19 at the 2024 American Society
of Clinical Oncology (ASCO) Annual Meeting and at the 2024 American
Transplant Congress (ATC).
The details for each meeting are as follows:
2024 ASCO Annual Meeting (May 31 – June 4,
Chicago, IL)
- Abstract# 2532: A
phase 3 study to evaluate efficacy and safety of VYD222, an IgG1
monoclonal antibody for prevention of COVID-19 (CANOPY): Subset
analysis of participants with significant immune compromise in the
setting of solid tumor or hematologic malignancies.
- Poster Details:
Board #11, Hall A; Saturday, June 1 from 9:00 AM – 12:00 PM
CDT
2024 ATC (June 1 – June 5, Philadelphia,
PA)
- Abstract #A018:
Preliminary results for solid organ transplant patients enrolled in
CANOPY, a phase 3 study to evaluate efficacy and safety of VYD222,
an IgG1 monoclonal antibody for prevention of COVID-19.
- Poster Details:
Poster Hall, Exhibit Hall A‚ Level 2; Saturday, June 1 from 5:30 PM
– 7:00 PM EST
Copies of the posters will be available on the Invivyd website
under the ‘Scientific Publications’ section after the posters are
presented at the meetings.
About Invivyd
Invivyd, Inc. (Nasdaq: IVVD) is a biopharmaceutical company
devoted to delivering protection from serious viral infectious
diseases, beginning with SARS-CoV-2. The company’s proprietary
INVYMAB™ platform approach combines state-of-the-art viral
surveillance and predictive modeling with advanced antibody
engineering. INVYMAB is designed to facilitate the rapid, serial
generation of new monoclonal antibodies (mAbs) to address evolving
viral threats. In March 2024, Invivyd received emergency use
authorization (EUA) from the U.S. FDA for its first mAb in a
planned series of innovative antibody candidates. Visit
https://invivyd.com/ to learn more.
Contacts:
Media Relations(781) 208-0160media@invivyd.com
Investor Relations(781) 208-0160investors@invivyd.com
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