ClinicalTrials.gov record
Active, not recruiting Phase 1 Interventional

AZD9291 in Combination With Ascending Doses of Novel Therapeutics

ClinicalTrials.gov ID: NCT02143466

Public ClinicalTrials.gov record NCT02143466. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 8, 2026, 5:06 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-arm, Phase Ib, Open-Label, Multicentre Study to Assess the Safety,Tolerability, Pharmacokinetics and Preliminary Anti-tumour Activity of AZD9291 in Combination With Ascending Doses of Novel Therapeutics in Patients With EGFRm+ Advanced NSCLC Who Have Progressed Following Therapy With an EGFR TKI (TATTON).

Study identification

NCT ID
NCT02143466
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 1
Lead sponsor
AstraZeneca
Industry
Enrollment
344 participants

Conditions and interventions

Interventions

  • Part A - AZD9291 in combination with AZD6094 Drug
  • Part A - AZD9291 in combination with MEDI4736 Drug
  • Part A - AZD9291 in combination with continuous selumetinib (Asian subjects) Drug
  • Part A - AZD9291 in combination with continuous selumetinib (non-Asian subjects) Drug
  • Part A - AZD9291 in combination with intermittent selumetinib Drug
  • Part B - AZD9291 in combination with AZD6094 Drug
  • Part B - AZD9291 in combination with MEDI4736 Drug
  • Part B - AZD9291 in combination with selumetinib Drug
  • Part C - AZD6094 monotherapy (Japan only) Drug
  • Part C - AZD9291 in combination with AZD6094 (Japan only) Drug
  • Part D - AZD9291 in combination with AZD6094 Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 130 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 4, 2014
Primary completion
Mar 3, 2020
Completion
Dec 30, 2026
Last update posted
Apr 23, 2026

2014 – 2026

United States locations

U.S. sites
6
U.S. states
5
U.S. cities
5
Facility City State ZIP Site status
Research Site Atlanta Georgia 30329
Research Site Boston Massachusetts 02114
Research Site Boston Massachusetts 02215
Research Site New York New York 10065
Research Site Philadelphia Pennsylvania 19111
Research Site Nashville Tennessee 37232

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 36 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02143466, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 23, 2026 · Synced May 8, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02143466 live on ClinicalTrials.gov.

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