Study of TUB-040 for Ovarian Cancer and Non-Small Cell Lung Cancer

This study is testing a new treatment called TUB-040 for people with ovarian cancer or non-small cell lung cancer that has come back or hasn't responded to other treatments. TUB-040 is an antibody-drug conjugate, which means it's designed to deliver a cancer-fighting drug directly to tumor cells that have a specific marker called NaPi2b. The main goal is to find the safest and most effective dose of TUB-040. You might be able to join if you are 18 or older, your cancer can't be cured with current treatments, and you've already tried standard treatments. The study is currently unclear on its recruitment status and plans to enroll about 250 people.

Study design
This is an open-label study, meaning both you and your doctors will know which treatment you are receiving. It involves two parts: first, increasing doses of TUB-040 are given to find the highest safe dose, then different doses are compared to find the best one.
What's involved
TUB-040 is given as an intravenous (IV) solution on day 1 of each 21-day treatment cycle.
Compensation
Not stated in the trial record.
Follow-up
Your safety will be monitored from enrollment until 30 days after your last study drug dose.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06303505

FiH Study to Investigate Safety, PK and Efficacy of the NaPi2b ADC TUB-040 in Patients With PROC or r/r Adenocarcinoma NSCLC

Recruiting
PHASE1Ages 18+InterventionalTreatment
Tubulis GmbH
~250 participants
Updated 2026-08-17 on ClinicalTrials.gov
What's tested:TUB-040

At a glance

Recruiting sites
16 of 16 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Determination of MTD
Measured over From enrollment until 30 days after last study drug
Ovarian Cancer
Non-small Cell Lung Cancer
16 sites across 13 states
Ohio2
Germany2
Spain2
Alabama1
New York1
Oklahoma1
Texas1
Utah1
  • Yariv Houvras, MD, PhD · STUDY_DIRECTOR · Tubulis GmbH

Opens a ready-to-send draft in your own email app — review before sending.

  • Determination of MTDFrom enrollment until 30 days after last study drug

    The highest dose is defined at which no more than 1 of 3 patients have had a Dose Limiting Toxicity (DLT) according to NCI CTCAE V5.0 criteria