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Cancer drug olaparib gets a makeover: which pill works best?

NCT ID NCT00777582

First seen Jan 15, 2026 · Last updated Jun 19, 2026 · Updated 28 times

Summary

This phase I trial tests two different oral forms of the cancer drug olaparib (AZD2281) in people with advanced solid tumors that have not responded to standard treatments. The main goal is to see how well the body absorbs each form. About 197 participants will receive both forms in a random order to compare their bioavailability and safety.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Locations

  • Research Site

    Randwick, 2031, Australia

  • Research Site

    Leuven, 3000, Belgium

  • Research Site

    Bellinzona, CH-6500, Switzerland

  • Research Site

    Edinburgh, EH4 2XR, United Kingdom

  • Research Site

    London, NW1 2PG, United Kingdom

  • Research Site

    Manchester, M20 4BX, United Kingdom

  • Research Site

    Newcastle upon Tyne, NE7 7DN, United Kingdom

  • Research Site

    Northwood, HA6 2RN, United Kingdom

  • Research Site

    Oxford, OX3 7LE, United Kingdom

  • Research Site

    Sutton, SM2 5PT, United Kingdom

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

Olaparib (AZD2281)

What this could lead to

If successful, this could help identify the best oral form of olaparib for future use in cancer treatment.

What could go wrong

This is an early-phase trial focused on drug absorption, not on curing cancer. Results may not lead to improved outcomes for patients.

Conditions

The condition(s) this trial relates to.

neoplasm

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.