Alkermes Announces Two Abstracts Accepted for Presentation at 2021 American Society of Clinical Oncology Annual Meeting

<br /> Alkermes Announces Two Abstracts Accepted for Presentation at 2021 American Society of Clinical Oncology Annual Meeting<br />

– Two Posters to Include Data Updates From ARTISTRY-1 and ARTISTRY-2 Clinical Trials Evaluating Immuno-Oncology Candidate Nemvaleukin Alfa –

PR Newswire


DUBLIN

,

April 28, 2021

/PRNewswire/ —

Alkermes plc

(Nasdaq: ALKS) today announced the acceptance of two abstracts related to nemvaleukin alfa (nemvaleukin), the company’s novel, investigational engineered interleukin-2 (IL-2) variant immunotherapy, at the 2021 American Society of Clinical Oncology (ASCO) Annual Meeting, taking place virtually

June 4-8, 2021

. New data from the phase 1/2 ARTISTRY-1 clinical trial evaluating the tolerability and efficacy of nemvaleukin administered intravenously as a monotherapy and in combination with pembrolizumab (KEYTRUDA

®

) will be shared in a poster discussion session. In addition, data supporting the recommended phase 2 dose (RP2D) for nemvaleukin administered subcutaneously from the phase 1/2 ARTISTRY-2 clinical trial will be shared in a separate poster.

Details of the presentations are as follows:


Abstract:

2513


Title:

ARTISTRY-1: Nemvaleukin alfa monotherapy and in combination with pembrolizumab in patients (pts) with advanced solid tumors


Presenter:


Valentina Boni

, M.D., Ph.D., Medical Oncologist and Principal Investigator, START

Madrid

at Centro Integral Oncológico Clara Campal


Presentation Date/Time:

The on-demand poster discussion session will take place on

June 4, 2021

from 9:00 –

10:00 a.m. ET

.


Abstract:

2552


Title:

Selection of the recommended phase 2 dose (RP2D) for subcutaneous nemvaleukin alfa: ARTISTRY-2


Presenter:


Omid Hamid

, M.D., Chief of Research and Immunotherapy, The Angeles Clinic and Research Institute


Presentation Date:

The poster presentation will be available on-demand to attendees beginning

June 4, 2021

.



About Nemvaleukin alfa (“nemvaleukin”)



Nemvaleukin is an investigational, novel, engineered fusion protein comprised of modified interleukin-2 (IL-2) and the high affinity IL-2 alpha receptor chain, designed to selectively expand tumor-killing immune cells while avoiding the activation of immunosuppressive cells by preferentially binding to the intermediate-affinity IL-2 receptor complex. The selectivity of nemvaleukin is designed to leverage the proven anti-tumor effects of existing IL-2 therapy while mitigating certain limitations.



About the ARTISTRY Clinical Development Program



ARTISTRY is an Alkermes-sponsored clinical development program evaluating nemvaleukin alfa as a potential immunotherapy for cancer. The ARTISTRY program is comprised of multiple clinical trials evaluating intravenous and subcutaneous dosing of nemvaleukin, both as a monotherapy and in combination with the anti-PD-1 therapy KEYTRUDA

®

(pembrolizumab) in patients with advanced solid tumors. Ongoing trials include:

ARTISTRY-1

,

ARTISTRY-2

,

ARTISTRY-3

and

ARTISTRY-6

.



About Alkermes plc



Alkermes plc is a fully-integrated, global biopharmaceutical company developing innovative medicines in the fields of neuroscience and oncology. The company has a portfolio of proprietary commercial products focused on addiction and schizophrenia, and a pipeline of product candidates in development for schizophrenia, bipolar I disorder, neurodegenerative disorders and cancer. Headquartered in Dublin, Ireland, Alkermes plc has an R&D center in Waltham, Massachusetts; a research and manufacturing facility in Athlone, Ireland; and a manufacturing facility in Wilmington, Ohio. For more information, please visit Alkermes’


website at





www.alkermes.com




.

KEYTRUDA

®

is a registered trademark of Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, USA.


Alkermes Contacts:


For Investors:

Sandy Coombs

, +1 781 609 6377

For Media: Sourojit Bhowmick, Ph.D. +1 781 609 6397

Cision
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