Ask to take part

Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.

Contact Information:

Alexander Cowley, PhD +44 (0) 20 3437 6927
alexander.cowley@icr.ac.uk


Anna Zachariou, PhD anna.zachariou@icr.ac.uk


Study Location:

Skip to Main Content
English | Cymraeg
Be Part of Research - Trial Details - Combination Study of Guadecitabine/ASTX727 and Pembrolizumab

Combination Study of Guadecitabine/ASTX727 and Pembrolizumab

Recruiting

Open to: ALL

Age: 18.0 - N/A

Medical Conditions

Carcinoma, Non-Small-Cell Lung


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


HyPeR is a multi-centre Phase 1 Dose Escalation Study of Guadecitabine (SGI-110)/ASTX727 a Second Generation Hypo-Methylating Agent in Combination with Pembrolizumab (MK3475) in Patients with Refractory Solid Tumours. The investigators will be investigating the safety and toxicity of the combination.

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Jan 2017 Sep 2026

Publications

"Papadatos-Pastos D, Yuan W, Pal A, Crespo M, Ferreira A, Gurel B, Prout T, Ameratunga M, Chenard-Poirier M, Curcean A, Bertan C, Baker C, Miranda S, Masrour N, Chen W, Pereira R, Figueiredo I, Morilla R, Jenkins B, Zachariou A, Riisnaes R, Parmar M, Turner A, Carreira S, Yap C, Brown R, Tunariu N, Banerji U, Lopez J, de Bono J, Minchom A. Phase 1, dose-escalation study of guadecitabine (SGI-110) in combination with pembrolizumab in patients with solid tumors. J Immunother Cancer. 2022 Jun;10(6):e004495. doi: 10.1136/jitc-2022-004495."; "35717027"

INTERVENTIONAL

Intervention Type : DRUG
Intervention Description : In arm 1 (escalation) and 2 (expansion).

Intervention Arm Group : Escalation;Expansion;

Intervention Type : DRUG
Intervention Description : In arm 1 (escalation) and 2 (expansion).

Intervention Arm Group : B2: Lung Expansion;Escalation;Expansion;

Intervention Type : DRUG
Intervention Description : In arm B2 (lung expansion) replacing guadecitabine

Intervention Arm Group : B2: Lung Expansion;



You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Royal Marsden Hospital
    Sutton
    Surrey
    SM2 5PT
  • UCLH
    London
    W1T 7HA


The study is sponsored by Royal Marsden NHS Foundation Trust and is in collaboration with Astex Pharmaceuticals, Inc.; Merck Sharp & Dohme LLC; Institute of Cancer Research, United Kingdom.




We'd like your feedback

Your feedback is important to us. It will help us improve the quality of the study information on this site. Please answer both questions.


Is this study information helpful?

What will you do next?

Read full details for Trial ID: NCT02998567
Last updated 30 April 2025

This page is to help you find out about a research study and if you may be able to take part

You can print or share the study information with your GP/healthcare provider or contact the research team directly.