1. Antibody-drug Conjugate/ADC Related
  2. Antibody-Drug Conjugates (ADCs)
  3. Vobramitamab duocarmazine

Vobramitamab duocarmazine  (Synonyms: AEX4089DC1; MGC018)

Cat. No.: HY-145636
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Vobramitamab duocarmazine (AEX4089DC1; MGC018), a humanized antibody-drug conjugate (ADC) targeted against B7-H3 (CD276). Vobramitamab duocarmazine is comprised of the cleavable linker-Duocarmycin payload, Vc-seco-DUBA (HY-128957), conjugated to an anti-B7-H3 humanized IgG1κ monoclonal antibody. Vobramitamab duocarmazine has antineoplastic activity.

For research use only. We do not sell to patients.

Vobramitamab duocarmazine

Vobramitamab duocarmazine Chemical Structure

CAS No. : 2490556-51-7

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Description

Vobramitamab duocarmazine (AEX4089DC1; MGC018), a humanized antibody-drug conjugate (ADC) targeted against B7-H3 (CD276). Vobramitamab duocarmazine is comprised of the cleavable linker-Duocarmycin payload, Vc-seco-DUBA (HY-128957), conjugated to an anti-B7-H3 humanized IgG1κ monoclonal antibody. Vobramitamab duocarmazine has antineoplastic activity[1].

In Vitro

Vobramitamab duocarmazine (MGC018; for 7 days) exhibits cytotoxicity toward B7-H3-positive human tumor cell lines, including MDA-MB-468, A375.S2, PA-1, Calu-6, NCI-H1703, Hs700T, LN-229, and SW48 cancer cells, with IC50 values range of 181-1447 pM. Vobramitamab duocarmazine exhibited bystander killing of target-negative tumor cells when cocultured with B7-H3-positive tumor cells[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

Vobramitamab duocarmazine (MGC018; 3-6 mg/kg; i.v; single-dose) leads to a dose-dependent decrease in tumor growth of MDA-MB-468 triple-negative breast cancer xenografts[1].
Vobramitamab duocarmazine (MGC018; 3-10 mg/kg; i.v; single-dose) leads to a rapid tumor regression, with a 98% reduction in tumor volume in a triple-negative breast cancer patient-derived xenograft (PDX) model[1].
Vobramitamab duocarmazine (MGC018; 3-10 mg/kg; i.v; single-dose) shows antitumor activity in the PA-1 ovarian cancer xenografts. A reduction in tumor volume of 89%, 91%, and 43%, is observed following treatment with Vobramitamab duocarmazine at 10, 6, and 3 mg/kg, respectively[1].
Vobramitamab duocarmazine (MGC018; 1-3 mg/kg; i.v; single-dose) shows antitumor activity in A375.S2 melanoma xenografts[1].
Vobramitamab duocarmazine (MGC018; 3-10 mg/kg; i.v; single-dose) shows antitumor activity in Calu-6 lung cancer xenografts. A reduction in tumor volume of 91%, 84%, and 72% is observed following treatment with Vobramitamab duocarmazine at 10 mg/kg, 6 mg/kg, and 3 mg/kg, respectively[1].
Vobramitamab duocarmazine (MGC018; 3 mg/kg; QW×3 or Q2W×2; i.v) shows antitumor activity toward patient-derived xenograft models of prostate, and head and neck cancer displaying heterogeneous expression of B7-H3[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Female CD-1 nude (homozygous) mice (Crl:CD1-Foxn1nu) and female SCID/CES1c KO mice (5-7 weeks old) injected with MDA-MB-468 cells[1]
Dosage: 3 mg/kg, 6 mg/kg
Administration: Tail vein injection; a single-dose
Result: Led to a dose-dependent decrease in tumor growth of MDA-MB-468 triple-negative breast cancer xenografts.
Animal Model: Female Athymic Nude-Foxn1nu mice (triple-negative breast cancer models)[1]
Dosage: 3 mg/kg
Administration: Tail vein injection; once a week; for 2 weeks
Result: Led to a rapid tumor regression, with a 98% reduction in tumor volume.
CAS No.
SMILES

[Vobramitamab duocarmazine]

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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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