AZD9291 in Combination With Ascending Doses of Novel Therapeutics (NCT02143466)
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).
🩺 Plain-English Summary (8th-Grade Level)
The purpose of this study is to determine the safety, tolerability and preliminary anti-tumour activity of AZD9291 when given together with AZD6094 or selumetinib in patients with EGFR mutation positive advanced lung cancer
Who can join: Review the eligibility criteria below.
Location: Research Site — Atlanta, Georgia
Age range: 18 Years to 130 Years
🧪 Interventions in This Study
- Part A - AZD9291 in combination with AZD6094 (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 A - AZD9291 in combination with MEDI4736 (DRUG)
- Part B - AZD9291 in combination with AZD6094 (DRUG)
- Part B - AZD9291 in combination with selumetinib (DRUG)
- Part B - AZD9291 in combination with MEDI4736 (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)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (42 Sites)
Showing the first 25 of 42 sites.
- Research Site — Atlanta, Georgia
- Research Site — Boston, Massachusetts
- Research Site — Boston, Massachusetts
- Research Site — New York, New York
- Research Site — Philadelphia, Pennsylvania
- Research Site — Nashville, Tennessee
- Research Site — Calgary, Alberta
- Research Site — Edmonton, Alberta
- Research Site — Chūōku,
- Research Site — Habikino-shi,
- Research Site — Hirakata-shi,
- Research Site — Kashiwa,
- Research Site — Nagoya,
- Research Site — Nagoya,
- Research Site — Gdansk,
- Research Site — Krakow,
- Research Site — Olsztyn,
- Research Site — Poznan,
- Research Site — Warsaw,
- Research Site — Chelyabinsk,
- Research Site — Krasnoyarsk,
- Research Site — Moscow,
- Research Site — Omsk,
- Research Site — Saint Petersburg,
- Research Site — Saint Petersburg,
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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💡 How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.