AML (Acute Myelogenous Leukemia)AMLNCT06993883
Use of Venetoclax , AML , Sohag , Egypt
An observational study of AML (Acute Myelogenous Leukemia), run by Sohag University at 1 site in Egypt.
Trial summary
retrospective observational study to evaluate the benefit of adding venetoclax to chemotherapy in the first or second line setting in Sohag governorate. Read more about this study
- Who is it for?
- Ages 18 to 80 years
- Conditions the study is for
- AML (Acute Myelogenous Leukemia)
- What is being tested?
- Venetoclax
- How many people
- 43 participants
- Where
- 1 siteEgypt
- Study dates
- 1 Mar 2023to 30 Apr 2025
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 80 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: observational descriptive study
Who may be able to join
- Patients aged between 18 and 80 years.
- Pathological confirmation of AML.
- Use of venetoclax plus chemotherapy as a 1st versus 2nd line treatment.
Who cannot join
- age < 18 years age > 80 years other types of acute leukemia
- -
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Use of Venetoclax in AML Patients Retrospective Experience in Sohag Governorate , an Area of Limited Resources in Upper Egypt
retrospective observational study to evaluate the benefit of adding venetoclax to chemotherapy in the first or second line setting in Sohag governorate.
Read the detailed description
Acute Myeloid Leukaemia (AML) is an aggressive and most common hematologic malignancy in adults with a higher incidence in older adults with a median age of diagnosis of 68 years. It accounts for the largest number of annual deaths from leukaemia. Several new therapies have been approved after many years and are expected to impact patient outcomes, especially in patients aged 60 and above.
The standard treatment strategy for newly diagnosed AML is an intensive curative chemotherapy, and a combination of cytarabine (AraC) and anthracycline is recommended as remission induction therapy. However, many AML patients are ineligible for intensive therapy because of advanced age or co-morbidities. Treatment options are limited for these patients, especially older patients, who account for a large proportion of patients with newly diagnosed AML Venetoclax is an orally available, small-molecule selective B cell leukemia/lymphoma-2 ( BCL-2 ) inhibitor. In two placebo-controlled Phase 3 trials, the safety and efficacy of venetoclax-based therapy were confirmed in treatment-naive patients with AML who were ineligible for intensive chemotherapy owing to advanced age or comorbidities. In the VIALE-A study, the venetoclax plus azacitidine (AZA) arm demonstrated significantly better outcomes compared with the placebo plus AZA arm. In the VIALE-C study, the venetoclax plus LDAC arm did not meet its primary endpoint of a statistically significant improvement in overall survival compared with the placebo plus LDAC arm In November 2018, the US Food and Drug Administration granted accelerated approval for venetoclax in combination with AZA, decitabine or LDAC for the treatment of newly diagnosed AML in adults aged ≥75 years or who have co-morbidities that preclude the use of intensive induction chemotherapy.
Primary refractory disease and relapse remain the main obstacles for cure in AML. In fit patients several options based on higher doses of cytarabine have been published, with complete remission (CR) rates ranging from 40-55%. The BCL2 inhibitor venetoclax has demonstrated impressive antileukemic activity when combined with hypomethylating agents or low-dose cytarabine in newly diagnosed unfit AML patients, the addition of venetoclax to aggressive chemotherapy protocols as a second line in patients with refractory/ relapsed AML patients who are fit for such treatment gives marked advance in treating such difficult situation.
Even in some patients who show great side effects while using first line aggressive treatment , second line use of venetoclax combined with hypomethylating agents as a lower intensity second line option could give a great advance and safe method as a bridge to bone marrow transplantation and cure.
- Conditions
- AML (Acute Myelogenous Leukemia)
- Being tested
- Venetoclax
- Keywords
- AML, venetoclax, Sohag, Egypt
- Medical subject headings
- Leukemia, Myeloid, Acute
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
VenetoclaxDrug
observational study for the result of venetoclax use combined with chemotherapy in AML patients in Sohag governorate
| Study group | Role | What they receive |
|---|---|---|
| 1st line | newly diagnosed AML patients unfit for aggressive chemotherapy who received reduced intensity protocols plus venetoclax in the 1st line setting. Receives: Drug: Venetoclax | |
| 2nd line | refractory recurrent AML patients after 1st line chemotherapy who received venetoclax plus 2nd line chemotherapy. Receives: Drug: Venetoclax | |
| 3rd line | refractory recurrent AML patients after 2 lines chemotherapy who received venetoclax plus 3rd line chemotherapy. Receives: Drug: Venetoclax |
What is being measured
The primary outcome is the main question the study is designed to answer.
response rate
Measured: through the study completion an average 1.5 years
Secondary outcomes (1)
overall survival
survival from diagnosis till study end or death
Measured: 1.5 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted29 May 2025
- Study start1 Mar 2023
- Primary completion30 Apr 2025
- Study completion30 Apr 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for AML (Acute Myelogenous Leukemia)Studies of the same condition, open and under way.
- More trials run by Sohag UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Retrospective
- Enrolment
- 43 participants (actual)
Sponsor and investigators
- Lead sponsor
- Sohag University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Walaa Gamal Mohamed Soliman, Sohag University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06993883
- Sponsor's protocol ID
- Soh-Med-25-4-11PD
- Acronym
- AML
- Status last verified
- May 2025
- First submitted
- 13 May 2025
- Last updated
- 29 May 2025
- Results posted
- No
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 29 May 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Use of Venetoclax in AML Patients Retrospective Experience in Sohag Governorate , an Area of Limited Resources in Upper Egypt
- ClinicalTrials.gov ID
- NCT06993883
- Acronym / sponsor ID
- AML / Soh-Med-25-4-11PD
- Conditions
- AML (Acute Myelogenous Leukemia)
- Keywords
- AML, venetoclax, Sohag, Egypt
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 43 participants (actual)
- Lead sponsor
- Sohag UniversityUniversity, hospital or other
- Study start
- 1 Mar 2023 (actual)
- Primary completion
- 30 Apr 2025 (actual)
- Study completion
- 30 Apr 2025 (actual)
- First posted
- 29 May 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
retrospective observational study to evaluate the benefit of adding venetoclax to chemotherapy in the first or second line setting in Sohag governorate.
Detailed description
Acute Myeloid Leukaemia (AML) is an aggressive and most common hematologic malignancy in adults with a higher incidence in older adults with a median age of diagnosis of 68 years. It accounts for the largest number of annual deaths from leukaemia. Several new therapies have been approved after many years and are expected to impact patient outcomes, especially in patients aged 60 and above.
The standard treatment strategy for newly diagnosed AML is an intensive curative chemotherapy, and a combination of cytarabine (AraC) and anthracycline is recommended as remission induction therapy. However, many AML patients are ineligible for intensive therapy because of advanced age or co-morbidities. Treatment options are limited for these patients, especially older patients, who account for a large proportion of patients with newly diagnosed AML Venetoclax is an orally available, small-molecule selective B cell leukemia/lymphoma-2 ( BCL-2 ) inhibitor. In two placebo-controlled Phase 3 trials, the safety and efficacy of venetoclax-based therapy were confirmed in treatment-naive patients with AML who were ineligible for intensive chemotherapy owing to advanced age or comorbidities. In the VIALE-A study, the venetoclax plus azacitidine (AZA) arm demonstrated significantly better outcomes compared with the placebo plus AZA arm. In the VIALE-C study, the venetoclax plus LDAC arm did not meet its primary endpoint of a statistically significant improvement in overall survival compared with the placebo plus LDAC arm In November 2018, the US Food and Drug Administration granted accelerated approval for venetoclax in combination with AZA, decitabine or LDAC for the treatment of newly diagnosed AML in adults aged ≥75 years or who have co-morbidities that preclude the use of intensive induction chemotherapy.
Primary refractory disease and relapse remain the main obstacles for cure in AML. In fit patients several options based on higher doses of cytarabine have been published, with complete remission (CR) rates ranging from 40-55%. The BCL2 inhibitor venetoclax has demonstrated impressive antileukemic activity when combined with hypomethylating agents or low-dose cytarabine in newly diagnosed unfit AML patients, the addition of venetoclax to aggressive chemotherapy protocols as a second line in patients with refractory/ relapsed AML patients who are fit for such treatment gives marked advance in treating such difficult situation.
Even in some patients who show great side effects while using first line aggressive treatment , second line use of venetoclax combined with hypomethylating agents as a lower intensity second line option could give a great advance and safe method as a bridge to bone marrow transplantation and cure.
Study design
- Observational model
- Cohort
- Time perspective
- Retrospective
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| 1st line | – | Drug: Venetoclaxnewly diagnosed AML patients unfit for aggressive chemotherapy who received reduced intensity protocols plus venetoclax in the 1st line setting. |
| 2nd line | – | Drug: Venetoclaxrefractory recurrent AML patients after 1st line chemotherapy who received venetoclax plus 2nd line chemotherapy. |
| 3rd line | – | Drug: Venetoclaxrefractory recurrent AML patients after 2 lines chemotherapy who received venetoclax plus 3rd line chemotherapy. |
Who may qualify
- Ages
- 18 to 80 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- observational descriptive study
Key inclusion criteria (3 listed)
- Patients aged between 18 and 80 years.
- Pathological confirmation of AML.
- Use of venetoclax plus chemotherapy as a 1st versus 2nd line treatment.
Key exclusion criteria (2 listed)
- age < 18 years age > 80 years other types of acute leukemia
- -
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Venetoclaxobservational study for the result of venetoclax use combined with chemotherapy in AML patients in Sohag governorate | Drug | 1st line, 2nd line, 3rd line |
Primary outcome
response rate
Time frame: through the study completion an average 1.5 years
1 secondary outcome
overall survival
Time frame: 1.5 years
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 29 May 2025.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of AML (Acute Myelogenous Leukemia), run by Sohag University at 1 site in Egypt.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 29 May 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
response rate (time frame: through the study completion an average 1.5 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 May 2025.