A Phase I First-in-Human Study of ABBV-011, a Seizure-Related Homolog Protein 6-Targeting Antibody-Drug Conjugate, in

Daniel Morgensztern1, Neal Ready2, Melissa L Johnson3

  • 1Washington University School of Medicine, St. Louis, Missouri.

Abstract

Insights

ABBV-011, a novel antibody targeting Seizure-related homolog protein 6 (SEZ6), showed promising antitumor activity in patients with relapsed/refractory small cell lung cancer (SCLC). This SEZ6-targeted therapy was well tolerated and warrants further investigation in SCLC treatment.

Area of Science:

  • Oncology
  • Pharmacology
  • Immunotherapy

Background:

  • Small cell lung cancer (SCLC) remains a challenging malignancy with limited treatment options for relapsed/refractory disease.
  • Seizure-related homolog protein 6 (SEZ6) is identified as a novel therapeutic target in SCLC.
  • ABBV-011 is a novel antibody-drug conjugate targeting SEZ6, delivering calicheamicin to cancer cells.

Purpose of the Study:

  • To evaluate the safety, tolerability, and preliminary antitumor activity of ABBV-011 monotherapy in patients with relapsed/refractory SCLC.
  • To determine the maximum tolerated dose (MTD) and recommended dose for expansion of ABBV-011.
  • To assess the pharmacokinetic profile of ABBV-011 in this patient population.

Main Methods:

  • A Phase I study (NCT03639194) involving dose escalation and expansion cohorts.
  • Intravenous administration of ABBV-011 every 3 weeks.
  • Preselection of patients with SEZ6-positive tumors (≥25% tumor cells with ≥1+ staining intensity by IHC) for the expansion phase.

Main Results:

  • 99 patients received ABBV-011 monotherapy; MTD was not reached up to 2.0 mg/kg.
  • Common treatment-emergent adverse events included fatigue (50%), nausea (42%), and thrombocytopenia (41%).
  • Objective response rate (ORR) was 19% overall, and 25% in the 1 mg/kg expansion cohort. Median response duration was 4.2 months.

Conclusions:

  • ABBV-011 monotherapy at 1.0 mg/kg every 3 weeks was well tolerated in heavily pretreated SCLC patients.
  • The study demonstrated encouraging antitumor activity, supporting SEZ6 as a promising SCLC target.
  • Further investigation of ABBV-011 in SCLC is warranted.