Marker Therapeutics to Host Clinical Program Update Conference Call and Webcast on Wednesday, February 16, 2022

Rhea-AI Summary

Marker Therapeutics, Inc. (Nasdaq:MRKR) announced a conference call and webcast on February 16, 2022, at 5:00 p.m. EST to discuss updates on its clinical programs and pipeline. The event will be accessible via the Investors section of the company's website. Marker specializes in next-generation T cell-based immunotherapies for hematological malignancies and solid tumors, focusing on non-engineered, tumor-specific T cells. The company believes its therapies are easier to manufacture and less toxic than current CAR-T and TCR approaches, potentially providing significant clinical benefits.

HOUSTON, Feb. 08, 2022 (GLOBE NEWSWIRE) -- Marker Therapeutics, Inc. (Nasdaq:MRKR), a clinical-stage immuno-oncology company specializing in the development of next-generation T cell-based immunotherapies for the treatment of hematological malignancies and solid tumor indications, today announced that it will host a conference call and webcast on Wednesday, February 16, 2022 at 5:00 p.m. EST to provide an update on the Company’s clinical programs, manufacturing processes and pipeline.

The webcast will be accessible in the Investors section of the Company's website at www.markertherapeutics.com. Individuals can participate in the conference call by dialing 877-869-3847 (domestic) or 201-689-8261 (international) and referring to the "Marker Therapeutics Clinical Program Update Call."

The archived webcast will be available for replay on the Marker website following the event.

About Marker Therapeutics, Inc.
Marker Therapeutics, Inc. is a clinical-stage immuno-oncology company specializing in the development of next-generation T cell-based immunotherapies for the treatment of hematological malignancies and solid tumor indications. Marker’s cell therapy technology is based on the selective expansion of non-engineered, tumor-specific T cells that recognize tumor associated antigens (i.e. tumor targets) and kill tumor cells expressing those targets. This population of T cells is designed to attack multiple tumor targets following infusion into patients and to activate the patient’s immune system to produce broad spectrum anti-tumor activity. Because Marker does not genetically engineer its T cell therapies, we believe that our product candidates will be easier and less expensive to manufacture, with reduced toxicities, compared to current engineered CAR-T and TCR-based approaches, and may provide patients with meaningful clinical benefit. As a result, Marker believes its portfolio of T cell therapies has a compelling product profile, as compared to current gene-modified CAR-T and TCR-based therapies.

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IR and Media Contacts

Marker Therapeutics:

Neda Safarzadeh
Vice President/Head of Investor Relations, PR & Marketing
(713) 400-6451
investor.relations@markertherapeutics.com

Solebury Trout:

Investors
Xuan Yang
xyang@soleburytrout.com

Media
Amy Bonanno
abonanno@soleburytrout.com

FAQ

What are the details of the Marker Therapeutics conference call on February 16, 2022?

Marker Therapeutics will host a conference call on February 16, 2022, at 5:00 p.m. EST to provide updates on its clinical programs and pipeline.

Where can I access the Marker Therapeutics conference call and webcast?

The conference call and webcast can be accessed in the Investors section of Marker Therapeutics' website.

What is the focus of Marker Therapeutics' clinical development?

Marker Therapeutics focuses on developing next-generation T cell-based immunotherapies for treating hematological malignancies and solid tumors.

How does Marker Therapeutics differentiate its T cell therapies from others?

Marker Therapeutics' T cell therapies are based on non-engineered, tumor-specific T cells, which they believe are easier and less expensive to manufacture than engineered therapies.

What potential advantages do Marker Therapeutics' treatments offer?

Marker Therapeutics claims their treatments may provide meaningful clinical benefits with reduced toxicities compared to current CAR-T and TCR-based therapies.