A Study to Find a Suitable Dose of ASP5834 in Adults With Solid Tumors
This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.
About the trial
Genes contain genetic code which tell the body which proteins to make. Many types of cancer are caused by changes, or mutations, in a gene called KRAS. Researchers are looking for ways to stop the actions of abnormal proteins made from the mutated KRAS gene. ASP5834 is being studied in people with solid tumors who have certain KRAS gene mutations. Some people with solid tumors of the colon or rectum (colorectal cancer), will be given ASP5834 with panitumumab. Panitumumab is a treatment for colorectal cancer. In this study, the researchers will learn how ASP5834 is processed by and acts upon the body. This information will help find a suitable dose of ASP5834 and check for any potential medical problems from the treatment. The main aims of this study are to check the safety of ASP5834 given by itself or given with panitumumab, and how well it is tolerated; and to find a suitable dose of ASP5834 given by itself or given with panitumumab. People in this study will be adults with locally advanced, unresectable, or metastatic solid tumors with certain KRAS gene mutations. Locally advanced means the cancer has spread to nearby tissue. Unresectable means the cancer cannot be removed by surgery. Metastatic means the cancer has spread to other parts of the body. They either haven't responded to standard treatment or couldn't be given standard treatment. The key reasons people cannot take part are if they have specific uncontrollable cancers such as symptomatic or untreated cancers in nervous system, have specific heart conditions, swelling and irritation of lung tissues (pneumonitis or interstitial lung disease, also called ILD), infections, or have recently had a stroke or a bleed on the brain. In this study, ASP5834 is being given to humans for the first time. This is an open-label study. This means that people in this study and clinic staff will know that they will receive ASP5834 by itself or ASP5834 with panitumumab. This study will be in 2 parts: Part 1 is called Dose Escalation. Different small groups of people will receive lower to higher doses of either: ASP5834 by itself or ASP5834 with panitumumab. Only people who have colorectal cancer will receive ASP5834 with panitumumab. People with any type of solid tumor will receive ASP5834 by itself. For each dose, all medical problems will be recorded. A medical expert panel will check the results and decide if the next group can receive a higher dose of ASP5834. The panel will do this until the planned maximum number of people are treated or until suitable doses have been selected for Part 2. Part 2 is called Dose Expansion. Other different small groups of people will receive ASP5834 or ASP5834 with panitumumab. They will receive the most suitable doses worked out from Part 1. In both parts of the study, the study treatments ASP5834 and panitumumab will be given through a vein. This is called an infusion. Each study treatment cycle is either 21 days or 28 days long. People will continue study treatment until: they have medical problems from the study treatment they can't tolerate; their cancer gets worse; they start other cancer treatment; or they ask to stop study treatment. People will visit the clinic on certain days during their study treatment, with extra visits during the first 2 cycles of study treatment. The study doctors will check for any medical problems from ASP5834. Also, people in the study will have a health check. On some visits they will also have scans to check for any changes in their cancer. Tumor samples will be taken at certain visits during study treatment with the option of a tumor sample being taken if people's cancer gets worse or the cancer comes back. People will visit the clinic shortly after stopping treatment for a health check. After this, people will have health checks every couple of months to check the condition of their cancer. The number of visits and checks done will depend on the health of each person and whether they completed their study treatment or not. It is expected that people will be in this study for about 1 year.
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Dorosły pacjent z zaawansowanym nowotworem, który nie można usunąć chirurgicznie lub który rozprzestrzenił się na inne części ciała
- •Potwierdzony nowotwór litego typu z określoną mutacją genu KRAS (G12V, G12D, G12C, G12R, G12A, G13D) lub zwielokrotnieniem genu KRAS
- •W części pierwszego etapu: pacjent, który otrzymał już standardowe leczenie zaawansowanego nowotworu
- •W części drugiego etapu z rakiem trzustki: potwierdzony zaawansowany rak trzustki (nieoperacyjny lub rozprzestrzeniający się)
- •W części drugiego etapu z rakiem trzustki: wcześniejsze leczenie obejmujące chemioterapię gemcytabinową lub fluoropirymidynową
✗ Disqualifies
- •Niekontrolowany rak ośrodkowego układu nerwowego lub symptomatyczne przerzuty do mózgu
- •Poważne problemy z sercem mogące wpłynąć na bezpieczeństwo
- •Zapalenie lub zwłóknienie płuc (pneumonitis lub ILD)
- •Aktywne infekcje
- •Niedawny udar lub krwawienie w mózgu
Simplified criteria — AI translation
Trial details
- Minimum age
- 18 Years
- Last updated (source)
- October 13, 2026
- Sex
- No restrictions
Therapies / drugs in trial
Locations (20)
UCLA Santa Monica Hematology Oncology
Santa Monica, United States
Winship Cancer Institute at Emory University
Atlanta, United States
Ochsner Health
Jefferson, United States
START Midwest
Grand Rapids, United States
Washington University School of Medicine
St Louis, United States
Hackensack University Medical Center
Hackensack, United States
Roswell Cancer Institute
Buffalo, United States
Memorial Sloan Kettering Cancer Center
New York, United States
University Hospitals - UH Cleveland Medical Center
Cleveland, United States
NEXT Oncology Dallas
Irving, United States
NEXT Oncology Virginia
Fairfax, United States
Site FR33003
Bordeaux, France
Site FR33002
Lyon, France
Site FR33004
Pierre-Bénite, France
Site FR33001
Villejuif, France
Kansai Medical University Hospital
Hirakata, Japan
Cancer Institute Hospital of JFCR
Koto-ku, Japan
Site ES34005
Barcelona, Spain
Site ES34001
Madrid, Spain
Site ES34003
Madrid, Spain
Trial contact
Astellas Pharma Global Development, Inc.
Contact information from ClinicalTrials.gov. Contact in English.
Share this trial
Data from ClinicalTrials.gov. AI-assisted translation, last sync: 10/14/2026.
You can help another person
We fund the Radar, this site, and the development of our Grosz dla Życia fundraising platform from donations and our own resources. Every contribution, even a small one, really helps.