Medicenna Announces Results of Annual Meeting of Shareholders
Medicenna is pleased to announce that all of the nominees listed in the management proxy circular dated August 2, 2022 were elected as directors. Each of the directors was elected with greater than 97% of the votes cast by shareholders present at the Meeting or represented by proxy. The results of the vote are detailed below:
Nominee | Votes For | % of Votes For |
Votes Against |
% of Votes Against |
Dr. |
24,859,038 | 97.878 | 538,956 | 2.122 |
Mr. |
24,877,225 | 97.950 | 520,768 | 2.050 |
Ms. |
24,902,175 | 98.048 | 495,818 | 1.952 |
Dr. |
24,728,697 | 97.365 | 669,296 | 2.635 |
Ms. |
24,653,185 | 97.067 | 744,808 | 2.933 |
Dr. |
24,820,996 | 97.728 | 576,997 | 2.272 |
Dr. |
24,840,678 | 97.806 | 557,315 | 2.194 |
Medicenna shareholders also voted to appoint PricewaterhouseCoopers LLP as auditor of the Company.
A total of 57.468% of the issued and outstanding common shares of the Company were represented in person and by proxy at the Meeting.
About Medicenna
Medicenna is a clinical stage immunotherapy company focused on the development of novel, highly selective versions of IL-2, IL-4 and IL-13 Superkines and first in class Empowered Superkines. Medicenna's long-acting IL-2 Superkine, MDNA11, is a next-generation IL-2 with superior CD122 (IL-2 receptor beta) binding without CD25 (IL-2 receptor alpha) affinity thereby preferentially stimulating cancer killing effector T cells and NK cells. Medicenna’s early-stage BiSKITs™ program, (Bifunctional SuperKine ImmunoTherapies) is designed to enhance the ability of Superkines to treat immunologically “cold” tumors. Medicenna's IL-4 Empowered Superkine, MDNA55, has been studied in 5 clinical trials including a Phase 2b trial for recurrent GBM, the most common and uniformly fatal form of brain cancer. MDNA55 has obtained Fast-Track and Orphan Drug status from the FDA and FDA/EMA, respectively.
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Source: Medicenna Therapeutics Corp.