← Eichor
Study identifier: NCT07374419 Synced from ClinicalTrials.gov · July 30, 2026
● Recruiting

Atamparib in Patients With Advanced Solid Tumors

Condition: NSCLC Adenocarcinoma · Solid Tumor  ·  Sponsor: Nerviano Medical Sciences (Shanghai) Ltd.

PhasePhase 1/Phase 2
Planned participants178
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a multi-part, open-label, non-randomized phase Ib/II clinical trial designed to evaluate the safety, tolerability, pharmacokinetics, and preliminary antitumor activity of atamparib, an investigational agent, in patients with advanced or metastatic non-small cell lung cancer (NSCLC) adenocarcinoma. The study comprises dose escalation (phase Ib) and expansion (phase II).

This description comes directly from the study's public registry record.

Talk to the study team

Olivia Chi Operations Program Lead, Master  ·  86 18621117100  ·  olivia.chi@nervianoms.com

Qin Kang, Senior Project manager, Tigermed, bachelor  ·  86 158 5828 6160  ·  qin.kang@tigermedgrp.com

Always discuss trial participation with your own doctor first.

Locations (1)

Unit 3.53, 3rd Floor, No. 5, Lane 720 Cailun Road, Pilot Free Trade Zone, Shanghai, P.R.ChinaShanghai, Shanghai Municipality, ChinaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice. By subscribing you agree to our Terms of Use and Privacy Policy.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07374419