SEZ6-targeting antibody−drug conjugate ABBV-706 in advanced small cell lung cancer and solid tumors: a phase 1 trial - Summary - MDSpire
Coming Soon: Introducing MDSpire News. Learn more
Conexiant’s news site is now MDSpire News. Learn more

Phase 1 Trial of ABBV-706, an Antibody-Drug Conjugate Targeting SEZ6, in Patients with Advanced Small Cell Lung Cancer and Other Solid Tumors

  • By

  • Lauren Averett Byers

  • Byoung Chul Cho

  • Alissa J. Cooper

  • Anne C. Chiang

  • Ji-Youn Han

  • Muhammad Furqan

  • Afshin Dowlati

  • Daniel Morgensztern

  • Kyriakos P. Papadopoulos

  • Noura J. Choudhury

  • María Vieito

  • Jair Bar

  • Joo-Hang Kim

  • Wallace Akerley

  • Tae Min Kim

  • Young-Chul Kim

  • Luis Paz-Ares

  • Myung-Ju Ahn

  • Hiroshi Yokouchi

  • Darius Meiman

  • Wijith Munasinghe

  • Oluwadamilola Ogunyankin

  • Nadine Jahchan

  • Song Wang

  • Cristiano Ferlini

  • Randy R. Robinson

  • Frederick J. Kohlhapp

  • Tammy Palenski

  • Guillermo Rivell

  • Pooja Hingorani

  • Sreenivasa Chandana

  • June 1, 2026

Share

Objective:

The primary aim of this trial was to assess the safety, tolerability, pharmacokinetics, immunogenicity, and antitumor activity of ABBV-706 in patients suffering from relapsed or refractory solid tumors, with a particular focus on those diagnosed with relapsed or refractory small cell lung cancer (SCLC) and other advanced solid tumors.

Approach:
  • Study Design: This study was a first-in-human, open-label, phase 1 trial that involved adult patients with advanced solid tumors. Participants received ABBV-706 intravenously every three weeks.
  • Cohorts: The trial included several cohorts, such as dose-escalation and optimization cohorts specifically for patients with SCLC, a safety lead-in cohort, and expansion cohorts. The study evaluated specific dose levels of 1.8 mg/kg and 2.5 mg/kg.
  • Endpoints: The primary endpoints of the study were centered on safety and tolerability. Secondary endpoints were designed to evaluate pharmacokinetics, immunogenicity, and antitumor activity.
Key Findings:
  • ABBV-706 monotherapy exhibited a manageable safety profile, indicating that it can be administered without significant adverse effects.
  • The overall response rate (ORR) observed in the trial was 43.8%. Notably, the ORR was higher at 60.9% among patients with relapsed or refractory SCLC, suggesting a potential enhancement in efficacy compared to existing treatment options.
Interpretation:

The preliminary results from this trial indicate that ABBV-706 may have promising antitumor activity in patients with relapsed or refractory SCLC, highlighting the need for further investigation to validate these findings.

Limitations:
  • It is important to note that the study is still ongoing, and the results presented are preliminary.
  • The sample size for certain cohorts may restrict the generalizability of the findings, and potential biases inherent in the study design should be taken into account.
Conclusion:

ABBV-706 appears to be a promising treatment option for patients with relapsed or refractory SCLC, and further studies are warranted to confirm these initial findings and explore its potential in broader patient populations. ---

Original Source(s)

Related Content