Tidutamab

Modify Date: 2025-09-21 10:32:36

Tidutamab Structure
Tidutamab structure
Common Name Tidutamab
CAS Number 2148354-90-7 Molecular Weight N/A
Density N/A Boiling Point N/A
Molecular Formula N/A Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Tidutamab


Tidutamab (XmAb-18087) is a humanized and affinity-optimized bispecific antibody (bsAb) targeting SSTR2 binding domain and T-cell binding domain (CD3). Tidutamab possesses a full Fc domain to maintain long serum half-life.Tidutamab eliminates SSTR+ tumor cells by stimulating redirected T cellmediated cytotoxicity (RTcC)[1].

 Names

Name Tidutamab

 Tidutamab Biological Activity

Description Tidutamab (XmAb-18087) is a humanized and affinity-optimized bispecific antibody (bsAb) targeting SSTR2 binding domain and T-cell binding domain (CD3). Tidutamab possesses a full Fc domain to maintain long serum half-life.Tidutamab eliminates SSTR+ tumor cells by stimulating redirected T cellmediated cytotoxicity (RTcC)[1].
Related Catalog
In Vitro Tidutamab (XmAb-18087; 0-100000 ng/mL)与人 SSTR2+ CHO 细胞结合,ED50 值为 2.2 μg/mL,并介导 T 细胞杀伤 SSTR2+ 靶细胞[1]。
In Vivo Tidutamab (XmAb-18087; 3 mg/kg; i.p.; 单次注射) 在 NSG 小鼠中刺激人 T 细胞杀伤 SSTR2+ A549 肺癌肿瘤[1]。 Animal Model: NSG mice[1] Dosage: 3 mg/kg Administration: Intraperitoneal injection; single dose Result: lnduced anti-tumor activity in human PBMC-engrafted NSG mice.
References

[1]. Hyung LS, et, al. Anti-SSTR2 × anti-CD3 bispecific antibody induces potent killing of human tumor cells in vitro and in mice, and stimulates target-dependent T cell activation in monkeys: A potential immunotherapy for neuroendocrine tumors. Cancer Res (2017) 77 (13_Supplement): 3633.

 Chemical & Physical Properties

No Any Chemical & Physical Properties
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