Inmagene Initiates POC Study for Extended Half-Life OX40 mAb in Atopic Dermatitis

16 August 2023 | Wednesday | News


Inmagene Biopharmaceuticals ("Inmagene"), a clinical stage biotechnology company developing innovative and differentiated therapies for immunological and inflammatory diseases, announced that the first patient has been dosed in a global multicenter proof-of-concept (POC) study of IMG-007 in adult patients with moderate-to-severe atopic dermatitis (AD). The objective of the study is to assess the safety, pharmacokinetics, and efficacy of IMG-007 in AD patients. Additional information can be found at www.clinicaltrials.gov (NCT05984784).
Image Source : Public Domain

Image Source : Public Domain

IMG-007 is a humanized IgG1 monoclonal antibody (mAb) that specifically binds to the OX40 receptor. Its Fc region has been bioengineered, resulting in an extended half-life and a silenced antibody-dependent cell-mediated cytotoxicity (ADCC) function. In a single ascending dose study in healthy adults, IMG-007 demonstrated a half-life that exceeds the average half-life for conventional IgG antibodies. At anticipated therapeutic dose levels, target serum concentration is maintained for approximately 12-18 weeks after a single dose, which enables the potential for IMG-007 to be dosed every 12 weeks or less frequently, thereby potentially allowing long "drug holidays". IMG-007, up to 600 mg, was well tolerated with no serious or severe adverse events and no reports of pyrexia or chills.

"IMG-007 represents an investigational drug with multiple potential indications," said Yufang Lu, MD, PhD, Chief Medical Officer of Inmagene. "We are excited to begin this trial of IMG-007 in AD patients, following favorable safety and highly differentiated pharmacokinetic results of the earlier trial. We are continuing our evaluations of IMG-007's potential in other diseases where OX40 signaling pathway plays an important pathogenic role."

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