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MaxCyte and Wugen Sign Strategic Platform License to Expedite Scale-Up of Clinical and Commercial Manufacturing of Wugen’s Investigational Allogeneic, Off-the-Shelf Cell Therapies for Cancers

Key Takeaway: MaxCyte, Inc. and Wugen, Inc. have announced a strategic platform license agreement aimed at advancing Wugen's allogeneic, off-the-shelf cell therapies for cancers. Through this agreement, Wugen will utilize MaxCyte's Flow Electroporation technology and ExPERT platform for enhanced manufacturing capabilities. Wugen's lead therapy, WU-CART-007, is under evaluation for relapsed or refractory T-cell acute lymphoblastic leukemia, having received FDA orphan and fast-track designations. This partnership marks a significant step in developing innovative cancer treatments.

Market Sentiment Analysis

POSITIVE FACTORS

  • MaxCyte and Wugen have signed a strategic platform license to enhance cell therapy manufacturing.
  • Wugen's investigational therapies have received multiple FDA designations, enhancing their development prospects.
  • The collaboration is positioned to expedite progress in advancing new treatments for difficult-to-treat cancers.

Full Press Release Details

ROCKVILLE, Md. and ST. LOUIS, Jan. 30, 2024 (GLOBE NEWSWIRE) -- MaxCyte, Inc., (Nasdaq: MXCT; LSE: MXCT), a leading cell-engineering focused company providing enabling platform technologies to advance the discovery, development and commercialization of next-generation cell-based therapeutics and innovative bioprocessing applications, and Wugen, Inc., a clinical-stage biotechnology company developing allogeneic, off-the-shelf cell therapies to treat a broad range of hematological and solid tumor malignancies, today announced the signing of a strategic platform license (SPL).
Under the terms of the agreement, Wugen gains non-exclusive clinical and commercial rights to use MaxCyte’s Flow Electroporation® technology and ExPERT™ platform. In return, MaxCyte will receive annual license fees and program-related revenue.
Wugen is developing the next generation of off-the-shelf memory natural killer (NK) and CAR-T cell therapies for cancer. The company’s investigational cell therapies originate from healthy donors and are further engineered to enhance their function of eliminating cancer cells. Wugen’s lead program is evaluating WU-CART-007, a CD7 targeted CAR-T cell therapy, in a global Phase 1/2 clinical trial for the treatment of relapsed or refractory (R/R) T-cell acute lymphoblastic leukemia (T-ALL)/lymphoblastic lymphoma (LBL) in adolescent and adult patients. WU-CART-007 has received Orphan Drug, Fast Track, and Rare Pediatric Disease Designations from the U.S. Food and Drug Administration for the treatment of R/R T-ALL/LBL. Additional information is available on clinicaltrials.gov, identifier NCT# 04984356.
“As WU-CART-007 is transferred onto the ExPERT platform and continues to progress in the clinic, we are able to support efficient and seamless expansion to large-scale manufacturing,” said Maher Masoud, President and CEO of MaxCyte. “By working with MaxCyte, Wugen can maximize the number of doses in each manufacturing run for later stage clinical development and potential commercial phase.”
“Our partnership with MaxCyte is an exciting step in advancing our groundbreaking therapies for difficult-to-treat cancers,” said Kumar Srinivasan, PhD, MBA, President and CEO of Wugen. “This collaboration brings us even closer to delivering life-saving treatments to patients with limited options. With MaxCyte's expertise, we're in a position to expedite progress through crucial development stages and make a significant impact on patients’ lives.”
MaxCyte’s ExPERT™ instrument portfolio represents the next generation of clinically validated electroporation technology for complex and scalable cell engineering. Offering high transfection efficiency, seamless scalability, and enhanced functionality, the ExPERT™ platform is crucial for enabling the next wave of biological and cellular therapeutics. Wugen is MaxCyte’s 26th clinical/commercial partnership overall, each of which generates pre-commercial milestone revenue, the vast majority of which includes sales-based payments.
Wugen, Inc. is a clinical-stage biotechnology company developing the next generation of off-the-shelf memory natural killer (NK) and CAR-T cell therapies for cancer. Wugen is leveraging its proprietary Moneta™ platform and deep genomic engineering expertise to pioneer a new class of memory NK cell therapies to treat hematological and solid tumor malignancies. For more information, please visit https://wugen.com/
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Frequently Asked Questions

What technology did Wugen license from MaxCyte?

Wugen licensed MaxCyte's Flow Electroporation® technology and ExPERT™ platform.

What is Wugen's lead investigational therapy?

Wugen's lead therapy is WU-CART-007, targeting CD7 for cancer treatment.

What designations has WU-CART-007 received?

WU-CART-007 has Orphan Drug, Fast Track, and Rare Pediatric Disease Designations.

How does the ExPERT platform benefit Wugen?

The ExPERT platform enables efficient large-scale manufacturing and maximizes doses.

What is the purpose of the strategic platform license?

The license allows Wugen to use MaxCyte's technology for clinical and commercial purposes.

Last updated: Jan 30, 2024