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I-Mab Announces First Patient Dosed in Phase 1/2a Clinical Trial of Anti-CD47 Antibody, TJC4, in China - The clinical study will evaluate the safety and preliminary efficacy of TJC4, in patients with relapsed or refracto

Key Takeaway: I-Mab Announces First Patient Dosed in Phase 1/2a Clinical Trial of Anti-CD47 Antibody, SHANGHAI, China, and ROCKVILLE, MD., April 2, 2020 I-Mab (the Company ) (Nasdaq: IMAB), a clinical stage biopharmaceutical company committed to the discovery, development and commercializati

Full Press Release Details

I-Mab Announces First Patient Dosed in Phase 1/2a Clinical Trial of Anti-CD47 Antibody,
SHANGHAI, China, and ROCKVILLE, MD., April 2, 2020 I-Mab
(the Company ) (Nasdaq: IMAB), a clinical stage biopharmaceutical company committed to the discovery, development and commercialization of novel or highly differentiated biologics to treat diseases with significant unmet medical needs,
particularly cancers and autoimmune disorders, today announced that the first patient was dosed with TJC4 in a Phase 1/2a clinical trial evaluating its use in treating patients with relapsed or refractory acute myeloid leukemia (r/r AML) or
myelodysplastic syndrome (MDS) in China. TJC4, also known as TJ011133, is an internally developed differentiated anti-CD47 monoclonal antibody that is designed to minimize inherent binding to normal red blood cells while preserving its strong
anti-tumor activity.
The clinical trial in China is a multi-center, open-label, single-arm study to evaluate the
safety, tolerability, pharmacokinetics/pharmacodynamics and preliminary efficacy of TJC4 as a monotherapy in patients with r/r AML and MDS (CXSL1900039; NCT04202003;). I-Mab is also conducting a Phase 1 trial
(NCT Number: NCT03934814) in the U.S. in patients with advanced solid tumors and lymphoma, with complete data from the dose escalation portion expected in the third quarter of 2020.
We have been at full speed conducting clinical development of TJC4 in both U.S. and China, said Dr. Joan Shen, CEO of I-Mab. Dosing the first patient in China represents another important milestone, both for our TJC4 program and for patients, as TJC4 stands out as a globally competitive, highly differentiated anti-CD47 asset
for cancer treatment. Together with the Phase 1 dose escalation study of TJC4 in the U.S., we continue to leverage our clinical development capabilities and expertise to facilitate clinical validation of TJC4 in China and the U.S.
CD47 is a glycoprotein
over-expressed in a wide variety of cancers and delivers a don t eat me signal to tumor-engulfing macrophages through its ligand SIRP , and is one of the most promising immuno-oncology targets after PD-1 and PDL1.
TJC4 is a differentiated anti-CD47 monoclonal antibody and designed to minimize inherent binding to
normal red blood cells by this class of monoclonal antibodies yet preserve its strong anti-tumor activities. Blockade of CD47 by TJC4 enables macrophages to engulf cancer cells. TJC4 recognizes a unique epitope on CD47 and exhibits minimal binding
to red blood cells. The hematologic safety advantage of TJC4 has been demonstrated in a series of robust pre-clinical and toxicological studies including those in cynomolgus monkeys, while it maintains superb
anti-tumor activities.
I-Mab (Nasdaq: IMAB) is a dynamic, global biotech company exclusively focused on developing novel or highly
differentiated biologics in the therapeutic areas of immuno-oncology and autoimmune diseases. I-Mab s mission is to bring transformational medicines to patients through innovation. I-Mab s innovative pipeline of more than 10 clinical and pre-clinical stage drug candidates is driven by the Company s
Fast-to-PoC (Proof-of-Concept) and Fast-to-Market
development strategies through internal R&D and global partnerships. The Company is on track to become a fully integrated end-to-end global biopharmaceutical company
with cutting-edge discovery platforms, proven pre-clinical and clinical development expertise, and world-class GMP manufacturing capabilities. I-Mab has offices in China
and the United States. For more information, please visit http://ir.i-mabbiopharma.com
Safe Harbor Statement
This press release contains statements that may constitute forward-looking statements pursuant to the safe harbor provisions
of the U.S. Private Securities Litigation Reform Act of 1995. These forward-looking statements can be identified by terminology such as will, expects, anticipates, aims, future,
intends, plans, believes, estimates, likely to and similar statements. Statements that are not historical facts, including statements about
I-Mab s beliefs, plans and expectations, are forward-looking statements. Forward-looking statements involve inherent risks and uncertainties. Further information regarding these and other risks is
included in I-Mab s filings with the SEC. All information provided in this press release is as of the date of this press release, and I-Mab does not undertake any
obligation to update any forward-looking statement, except as required under applicable law.
For more information, please contact:
Office line: +86 21 6057 8000
Burns McClellan, Inc. (Americas and Europe)
Office line: +1 212 213 0006
The Piacente Group, Inc. (Asia)
Office line: + 86 21 6039 8363
Burns McClellan, Inc.
Ryo Imai / Robert Flamm, Ph.D.
Office line: +1 212 213 0006
Last updated: Apr 2, 2020