Abstract 687TiP
Background
Delta-like 1 homolog protein (DLK1), also known as preadipocyte factor 1 (PREF-1) and fetal antigen 1 (FA1), is a transmembrane protein and an inhibitor of NOTCH1 signaling. It modulates a wide range of developmental processes where NOTCH signaling is critical including cellular proliferation, cell fate, and terminal differentiation. As a result of its role in developmental signaling, expression of DLK1 decreases as development proceeds, with limited expression in adult tissues, with the exception of adrenal and pituitary glands, and ovaries. DLK1 is highly expressed in several cancers, including adrenocortical, uterine, and testicular cancers as well as a subset of pancreatic, sarcoma, liver, and lung cancers. Taken together, this expression profile makes DLK1 an attractive candidate for targeted therapeutic approaches. TORL-4-500 is an antibody-drug conjugate (ADC) with a fully humanized immunoglobulin G1 (IgG1) monoclonal antibody (mAb) selective for DLK1 linked to monomethyl auristatin E (MMAE), an anti-mitotic agent via a cathepsin hydrolysable dipeptide valine-citrulline (vc) linker.
Trial design
TORL-4-500-001 is a two-part first in human study to characterize the safety, tolerability, and dose-limiting toxicities (DLT) and to determine the maximum tolerated dose (MTD) and recommended phase 2 dose (RP2D) of TORL-4-500 administered as monotherapy intravenously Q3W in patients with advanced cancer. Serum PK, immunogenicity, and antitumor activity will also be evaluated. Endpoints include frequency and severity of adverse events and objective response rate (ORR) based on RECIST v1.1 criteria. Correlative biomarker studies will evaluate the relationship of clinical benefit with blood and tissue biomarkers. This study is currently open with patients enrolling in dose escalation. Once the RP2D is established, dose expansion in DLK1+ indication-specific cohorts will commence.
Clinical trial identification
NCT06005740.
Editorial acknowledgement
Legal entity responsible for the study
TORL Biotherapeutics.
Funding
TORL Biotherapeutics.
Disclosure
J.W. Goldman: Financial Interests, Personal, Invited Speaker: AstraZeneca; Financial Interests, Personal, Advisory Board: Genentech, Eli Lilly, Janssen, AbbVie, Gritstone; Financial Interests, Institutional, Coordinating PI: AstraZeneca, Eli Lilly; Financial Interests, Institutional, Local PI: Genentech, Janssen, BMS, AbbVie. L.S. Rosen: Financial Interests, Institutional, Funding, PI at UCLA Health Hem/Onc for Inspirna trial, Institution receives research funding: Inspirna. A. Kung, A. Romero, I. Qazi, H. Dokainish, S. Letrent: Financial Interests, Personal, Stocks/Shares: TORL Bio. D. Slamon: Financial Interests, Personal and Institutional, Member of Board of Directors: TORL Bio.
Resources from the same session
630P - Debio 0123 + carboplatin (CP) for patients (pts) with advanced solid tumors: Safety, preliminary efficacy and determination of recommended phase II dose (RP2D)
Presenter: Hans Gelderblom
Session: Poster session 01
631P - Phase Ib expansion study of CX-5461 in patients with solid tumours and BRCA2 and/or PALB2 mutation
Presenter: Pamela Soberanis Pina
Session: Poster session 01
632P - Results from the first-in-human study of ATR inhibitor, IMP9064 monotherapy dose escalation in patients with advanced solid tumors
Presenter: Chia-Chi Lin
Session: Poster session 01
633P - First-in-human dose-escalation study of basroparib (STP1002) in patients with advanced-stage solid tumors
Presenter: Christopher Lieu
Session: Poster session 01
634P - First results from phase I/II study of CTS2190, a novel small-molecule inhibitor of type I PRMTs, in patients with advanced solid tumors
Presenter: Xiangdong Cheng
Session: Poster session 01
635P - The phase I dose-escalation study of TSN084, a multi-kinase inhibitor, in patients with advanced malignant tumors
Presenter: Jie Wang
Session: Poster session 01
636P - Tucatinib and trastuzumab in advanced cancers with HER2 mutations or amplification: A molecular screening and therapeutics (MoST) program substudy
Presenter: Benjamin Kong
Session: Poster session 01
637P - AC699, a novel chimeric estrogen receptor degrader, in a phase I study in breast cancer
Presenter: Erika Hamilton
Session: Poster session 01
638P - Final results of IMPACT 2, a randomized study evaluating molecular profiling and targeted agents in metastatic cancer at MD Anderson Cancer Center
Presenter: Apostolia Maria Tsimberidou
Session: Poster session 01
639P - Serial ctDNA profiling as a catalyst for tailored therapeutics in advanced cancer: Analysis of two precision medicine studies
Presenter: Sophie Cousin
Session: Poster session 01