New study tracks leukemia Drug's Real-Life impact
NCT ID NCT03987958
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study follows about 100 adults with acute myeloid leukemia (AML) who are already prescribed venetoclax by their doctors in Israel. Researchers will track how long patients live and how many achieve remission during routine care. The goal is to understand the drug's real-world effectiveness and safety outside of controlled trials.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Aug 2019
- Expected to finish
-
Jul 2027
An estimate. End dates often move.
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Participants with AML treated with venetoclax in routine clinical practice
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Participant diagnosed with Acute Myeloid Leukemia (AML) and is eligible to receive venetoclax per Israel Ministry of Health. * Participant who will be treated with venetoclax and the decision to treat with venetoclax is made by the physician prior to any decision regarding participation in this study. Exclusion Criteria: \- Participant participating in an interventional trial within 30 days prior to starting venetoclax treatment.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Acute myeloid leukemia are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Assuta Tel Aviv Medical Center /ID# 213371
Tel Aviv, Central District, 6971028, Israel
-
Bnai Zion Medical Center /ID# 213344
Haifa, 3339419, Israel
-
HaEmek Medical Center /ID# 213370
Afula, Haifa District, 1834111, Israel
-
Hadassah /ID# 213356
Jerusalem, Jerusalem, 91120, Israel
-
Meir Medical Center /ID# 213352
Kfar Saba, Central District, 4428164, Israel
-
Rabin Medical Center. /ID# 213343
Petah Tikva, 4941492, Israel
-
Rambam Health Care Campus /ID# 213355
Haifa, 3109601, Israel
-
Shaare Zedek Medical Center /ID# 228016
Jerusalem, Jerusalem, 91031, Israel
-
Soroka University Medical Center /ID# 213369
Beersheba, Southern District, 8443901, Israel
-
Tel Aviv Sourasky Medical Center /ID# 213354
Tel Aviv, Tel Aviv, 6423906, Israel
-
The Chaim Sheba Medical Center /ID# 213353
Ramat Gan, Tel Aviv, 5265601, Israel
-
ZIV Medical Center /ID# 229211
Safed, Northern District, 13100, Israel
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can an HDAC inhibitor wipe out residual leukemia cells?
- Can an experimental pill block a cancer-driving enzyme in hard-to-treat leukemia?
- Two-Drug combo targets leukemia that outsmarted its first treatment
- Tweaking donor cells may shield older transplant patients from a dangerous complication
- Can a drug and donor cells stop leukemia from returning after transplant?
- New drug combination targets Hard-to-Treat blood cancers