🏛️ Verified NIH Record • Updated 2026-08-03

Perioperative Durvalumab With Neoadjuvant ddMVAC or Gemcitabine/Cisplatin in Patients With Muscle-invasive Bladder Cancer (NIAGARA-2) (NCT06960577)

A Phase IIIb, Open-label, Single-arm, Global Study of Perioperative Durvalumab With Neoadjuvant ddMVAC or Gem/Cis in Patients With Muscle-invasive Bladder Cancer (NIAGARA-2)

🟢 Recruiting Phase3 💊 Investigational Drug / Biologic Sponsor: AstraZeneca

🩺 Plain-English Summary (8th-Grade Level)

The Phase IIIb NIAGARA-2 study aims to expand on the data from the Phase III NIAGARA study by investigating perioperative durvalumab in combination with investigator-selected cisplatin-based neoadjuvant chemotherapy (either ddMVAC or gemcitabine/cisplatin) in a clinical practice setting.

Who can join: Review the eligibility criteria below.

Location: Research Site — Chermside

Age range: 18 Years

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (59 Sites)

Showing the first 25 of 59 sites.

  • Research Site — Chermside,
  • Research Site — Elizabeth Vale,
  • Research Site — Heidelberg,
  • Research Site — Hong Kong,
  • Research Site — Kogarah,
  • Research Site — Macquarie University,
  • Research Site — Murdoch,
  • Research Site — Port Macquarie,
  • Research Site — St Leonards,
  • Research Site — Barretos,
  • Research Site — Jaú,
  • Research Site — Natal,
  • Research Site — Porto Alegre,
  • Research Site — Rio de Janeiro,
  • Research Site — Santo André,
  • Research Site — São José do Rio Preto,
  • Research Site — São Paulo,
  • Research Site — Hamilton, Ontario
  • Research Site — London, Ontario
  • Research Site — Ottawa, Ontario
  • Research Site — Montreal, Quebec
  • Research Site — Québec, Quebec
  • Research Site — Sherbrooke, Quebec
  • Research Site — Angers,
  • Research Site — Angers,

📞 Contact the Study Coordinator

Phone: (877) 240-9479

Email: information.center@astrazeneca.com

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 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.

💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
🏛️ View Official NIH Record ↗