Acute Myeloid LeukemiaNCT06536010
Clinical Trial Protocol for the Combined Use of VAG in the Treatment of ND-AML
A study testing Venetoclax 100 mg d1,200 mg d2,400 mg d3-28; in people with Acute Myeloid Leukemia, run by Yang Xiaotian at 1 site in China.
Trial summary
This is a clinical efficacy study evaluating the VAG regimen in the treatment of newly diagnosed acute myeloid leukemia (AML). The main objectives of the study are to assess the efficacy and safety of the VAG regimen and to explore the synergistic mechanisms of VAG in combating AML. Read more about this study
- Who is it for?
- Ages 18 to 75 years
- Conditions the study is for
- Acute Myeloid Leukemia
- What is being tested?
- Venetoclax 100 mg d1,200 mg d2,400 mg d3-28;
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 50 participants
- Where
- 1 siteChina
- Study dates
- 3 Nov 2021to 31 Jul 2028
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
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 75 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Age between 18 and 75 years, regardless of gender.
- Diagnosis of AML (excluding APL) according to the 2022 World Health Organization (WHO) diagnostic criteria.
- ECOG performance status of 0-2.
- For female participants of childbearing potential or male participants with female partners of childbearing potential, effective contraceptive measures must be taken throughout the entire treatment period and for 6 months after the treatment period.
- Expected survival of at least 3 months.
- Ability to understand and willingness to participate in the study, and signing an informed consent form.
Who cannot join
- Acute promyelocytic leukemia (M3 subtype).
- Central nervous system leukemia.
- Severe uncontrolled infection or other major diseases.
- Heart failure: Ejection fraction (EF) < 50%, New York Heart Association (NYHA) class II or above.
- Impaired liver or kidney function: Serum total bilirubin ≥ 2.0 mg/dl, AST ≥ 3 times the upper limit of normal, serum creatinine clearance rate (Ccr) ≥ 50 ml/min, arterial oxygen saturation (SpO2) < 92%.
- Human immunodeficiency virus (HIV) positive.
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- Active hepatitis B or C.
- Pregnant or lactating women.
- Other conditions in which the investigator deems the participant unsuitable for the study.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
China1 site, 1 recruiting
- Recruiting
Huai'an Second People's Hospital
Huai'an, Jiangsu, 210000
Xiaotian Yang, 15695110492, 15695110492@163.com
About this study
Official title: Clinical Trial Protocol for the Combined Use of Azacitidine, Venetoclax, and Granulocyte Colony-Stimulating Factor in the Treatment of Newly Diagnosed Acute Myeloid Leukemia (AML) (Phase IIb, Single-arm, Prospective, Single-center Study)
This is a clinical efficacy study evaluating the VAG regimen in the treatment of newly diagnosed acute myeloid leukemia (AML).
The main objectives of the study are to assess the efficacy and safety of the VAG regimen and to explore the synergistic mechanisms of VAG in combating AML.
Read the detailed description
This study is a single-arm, prospective, single-center phase IIb clinical efficacy study evaluating the therapeutic effects of azacitidine and venetoclax in combination with granulocyte colony-stimulating factor for the treatment of newly diagnosed acute myeloid leukemia (AML).
Acute myeloid leukemia (AML) is a malignant disease originating from myeloid hematopoietic stem/progenitor cells. It is highly aggressive, and patients have a very low survival rate. The 5-year survival rate for diagnosed AML patients is approximately 29%, with only 5-15% for patients aged 60 and above. Currently, the 3+7 regimen is the first-line induction chemotherapy for newly diagnosed AML patients, with about 60-80% of young patients (<60 years old) and 40-60% of elderly patients (≥60 years old) achieving complete remission (CR). However, among AML patients receiving the 3+7 regimen, those with poor physical condition or high-risk cytogenetics have a worse prognosis. Therefore, there is a need to explore new treatment regimens that are less intensive but still effective.
Venetoclax is an oral selective Bcl-2 inhibitor. Multiple studies and clinical trials have demonstrated that Venetoclax, in combination with demethylating agents or low-dose cytarabine (LDAC), has synergistic anti-tumor effects and achieves higher treatment response and disease-free survival rates in AML patients. The results of the VIALE-A study showed that the median overall survival (OS) time with Venetoclax plus Azacitidine (AZA) was 14.7 months compared to 9.6 months with Azacitidine alone (P<0.001). The median duration of remission was 17.5 months with Venetoclax plus Azacitidine compared to 13.4 months with Azacitidine alone, and the CR+CRi rates were 66.4% and 28.3%, respectively (P<0.001). This combination significantly improves the overall survival of AML patients, with high response rates and good safety profile. In October 2020, the U.S. Food and Drug Administration approved the use of Venetoclax in combination with Azacitidine, Decitabine, or LDAC for the treatment of newly diagnosed AML patients aged 75 years or older or those who are unfit for intensive induction chemotherapy due to comorbidities. The Venetoclax plus Azacitidine regimen was also included in the AML NCCN guidelines in 2020. However, while Venetoclax in combination with demethylating agents is recommended for the treatment of elderly AML patients, there is currently a lack of research data for its use in young AML patients. The results of a phase II clinical trial presented at the 2022 ASH Annual Meeting, evaluating Venetoclax plus hypomethylating agents in young adults with newly diagnosed AML and adverse ELN risk, showed a complete remission with incomplete hematologic recovery (CRc) rate of 78% after one cycle of treatment, with a minimal residual disease (MRD) negativity rate of 77%. After two cycles of treatment, the CRc rate was 91.9% with an MRD negativity rate of 82.3%. The CRc rates for favorable, intermediate, and adverse risk groups were 69.6%, 75.4%, and 61.3%, respectively. Although the combination of Venetoclax and demethylating agents has shown promising efficacy, there are still limitations such as adverse events including thrombocytopenia (46%), nausea (44%), constipation (43%), neutropenia (42%), febrile neutropenia (42%), diarrhea (41%), and tumor lysis syndrome (TLS), as well as suboptimal achievement of MRD negativity and depth of remission after induction therapy.
Granulocyte colony-stimulating factor (G-CSF) is expressed by almost all AML cells and binds to its receptor, G-CSFR. In pre-activation regimens, G-CSF induces tumor cells in the quiescent phase (G0/G1) to enter the proliferative phase (S phase), enhancing the cytotoxic effect of chemotherapy drugs on tumor cells, improving the efficacy of chemotherapy, and reducing adverse reactions. A study conducted by Tang Xiaowen's team at the First Affiliated Hospital of Soochow University on the efficacy and safety of decitabine (DAC) combined with HAAG in the treatment of newly diagnosed acute myeloid leukemia showed that after one cycle of DAC+HAAG induction therapy in 50 patients, 48 patients (96%) achieved complete remission (CR)/CR with incomplete blood count recovery (CRp)/CR with incomplete count recovery and incomplete marrow recovery (CRi), and 2 patients (4%) achieved partial remission (PR). The median time to recovery of white blood cell count, platelet count, and hemoglobin was 17.5 days, 19.0 days, and 20.0 days, respectively. Only 16% (8/50) and 6% (3/50) of patients experienced grade 3-4 infections and bleeding, while non-hematologic toxicities were mainly grade 1-2 and resolved after symptomatic treatment.
The combination of venetoclax and hypomethylating agents is the most common approach, which synergistically induces cell apoptosis and reduces MCL-1 levels, thereby overcoming resistance to BCL-2 inhibitors. Additionally, the combination interferes with the energy metabolism of leukemia cells and targets leukemia stem cells. However, there is currently no research on the combination of azacitidine, venetoclax, and G-CSF. The investigators has conducted a preliminary clinical study on the VAG regimen (azacitidine, venetoclax, and granulocyte colony-stimulating factor) for newly diagnosed AML, which has shown promising results. We plan to expand the sample size and further investigate its mechanism of tumor cell killing.
- Conditions
- Acute Myeloid Leukemia
- Being tested
- Venetoclax 100 mg d1,200 mg d2,400 mg d3-28;
- 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.
Venetoclax 100 mg d1,200 mg d2,400 mg d3-28;Drug
Also called AZA 75mg/m2 on days 1-7, G-CSF: 50-600ug/day, starting on day 1 (adjusted based on WBC count of 10-25*10E9/L)
VAG in the induction phase of the ND-AML treatment protocol
| Study group | Role | What they receive |
|---|---|---|
| VAG regimen in the treatment of newly diagnosed acute myeloid leukemia (AML) | Experimental | AZA: 75mg/m2 on days 1-7 VEN: 100mg on day 1, 200mg on day 2, 400mg on days 3-28 G-CSF: 50-600ug/day, starting on day 1 (adjusted based on WBC count of 10-25*10E9/L)
In the induction phase of the ND-AML treatment protocol, VEN+AZA+G-CSF is administered. At the end of the induction phase, the efficacy is evaluated. If the patient achieves complete remission (CR), the original treatment protocol is continued for consolidation. If the patient achieves partial remission (PR), the original treatment protocol is repeated for induction until the patient achieves CR or shows no response (NR), progressive disease (PD), or relapse (PR/NR/PD). If the patient shows no response or progressive disease, the study is concluded. Receives: Drug: Venetoclax 100 mg d1,200 mg d2,400 mg d3-28; |
What is being measured
The primary outcome is the main question the study is designed to answer.
Complete Remission (CR)
- No symptoms or signs of leukemia cell infiltration, normal or near-normal life; B. Blood counts: Hb ≥ 100g/L (males) or ≥ 90g/L (females and children), absolute neutrophil count ≥ 1.5 × 109/L, platelets ≥ 100 × 109/L. No leukemia cells in peripheral blood leukocyte classification; C. Bone marrow morphology: Less than or equal to 5% of myeloblasts (type I + type II) (primitive monocytes + immature monocytes or primitive lymphocytes + immature lymphocytes), normal red blood cells and megakaryocytes; D. No extramedullary leukemia (no lymphadenopathy, splenomegaly, skin/gum infiltration, testicular masses, central nervous system involvement).
Measured: The period of 2 months from the start of treatment.
Secondary outcomes (5)
Partial Remission (PR)
Myeloblasts (type I + type II) (primitive monocytes + immature monocytes or primitive lymphocytes + immature lymphocytes) > 5% but ≤ 20%; or one of the following criteria is met in clinical, blood counts, and bone marrow morphology for complete remission.
Measured: The period of 1 month from the start of treatment.
Complete Remission with incomplete blood count recovery (CRi)
PLT < 100 × 109/L or NE < 1.5 × 109/L. Other criteria for CR should be met.
Measured: The period of 1 month from the start of treatment.
Overall Response Rate (ORR)
CR+CRi+MLFS+PR
Measured: The period of 4 months from the start of treatment.
Morphologic leukemia-free state (MLFS)
< 5% of primitive cells in bone marrow; no immature cells with Auer rods; no persistent extramedullary leukemia; no requirement for normal blood cell recovery.
Measured: The period of 1 month from the start of treatment.
Overall survival, OS
The time from the start of treatment to death or the end of follow-up, evaluated at 2 years after treatment.
Measured: The period of 2 years from the start of treatment.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted2 Aug 2024
- Study start3 Nov 2021
- Primary completion31 Jul 2026 (estimated)
- Study completion31 Jul 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Acute Myeloid LeukemiaStudies of the same condition, open and under way.
- 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 50 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Yang Xiaotian
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, Yang Xiaotian, The Second People's Hospital of Huai'an
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06536010
- Sponsor's protocol ID
- HEYLL202403
- Status last verified
- Jul 2024
- First submitted
- 29 Jul 2024
- Last updated
- 2 Aug 2024
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 2 Aug 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Clinical Trial Protocol for the Combined Use of Azacitidine, Venetoclax, and Granulocyte Colony-Stimulating Factor in the Treatment of Newly Diagnosed Acute Myeloid Leukemia (AML) (Phase IIb, Single-arm, Prospective, Single-center Study)
- ClinicalTrials.gov ID
- NCT06536010
- Acronym / sponsor ID
- HEYLL202403
- Conditions
- Acute Myeloid Leukemia
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 50 participants (estimated)
- Lead sponsor
- Yang XiaotianUniversity, hospital or other
- Study start
- 3 Nov 2021 (actual)
- Primary completion
- 31 Jul 2026 (estimated)
- Study completion
- 31 Jul 2028 (estimated)
- First posted
- 2 Aug 2024 (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.
This is a clinical efficacy study evaluating the VAG regimen in the treatment of newly diagnosed acute myeloid leukemia (AML).
The main objectives of the study are to assess the efficacy and safety of the VAG regimen and to explore the synergistic mechanisms of VAG in combating AML.
Detailed description
This study is a single-arm, prospective, single-center phase IIb clinical efficacy study evaluating the therapeutic effects of azacitidine and venetoclax in combination with granulocyte colony-stimulating factor for the treatment of newly diagnosed acute myeloid leukemia (AML).
Acute myeloid leukemia (AML) is a malignant disease originating from myeloid hematopoietic stem/progenitor cells. It is highly aggressive, and patients have a very low survival rate. The 5-year survival rate for diagnosed AML patients is approximately 29%, with only 5-15% for patients aged 60 and above. Currently, the 3+7 regimen is the first-line induction chemotherapy for newly diagnosed AML patients, with about 60-80% of young patients (<60 years old) and 40-60% of elderly patients (≥60 years old) achieving complete remission (CR). However, among AML patients receiving the 3+7 regimen, those with poor physical condition or high-risk cytogenetics have a worse prognosis. Therefore, there is a need to explore new treatment regimens that are less intensive but still effective.
Venetoclax is an oral selective Bcl-2 inhibitor. Multiple studies and clinical trials have demonstrated that Venetoclax, in combination with demethylating agents or low-dose cytarabine (LDAC), has synergistic anti-tumor effects and achieves higher treatment response and disease-free survival rates in AML patients. The results of the VIALE-A study showed that the median overall survival (OS) time with Venetoclax plus Azacitidine (AZA) was 14.7 months compared to 9.6 months with Azacitidine alone (P<0.001). The median duration of remission was 17.5 months with Venetoclax plus Azacitidine compared to 13.4 months with Azacitidine alone, and the CR+CRi rates were 66.4% and 28.3%, respectively (P<0.001). This combination significantly improves the overall survival of AML patients, with high response rates and good safety profile. In October 2020, the U.S. Food and Drug Administration approved the use of Venetoclax in combination with Azacitidine, Decitabine, or LDAC for the treatment of newly diagnosed AML patients aged 75 years or older or those who are unfit for intensive induction chemotherapy due to comorbidities. The Venetoclax plus Azacitidine regimen was also included in the AML NCCN guidelines in 2020. However, while Venetoclax in combination with demethylating agents is recommended for the treatment of elderly AML patients, there is currently a lack of research data for its use in young AML patients. The results of a phase II clinical trial presented at the 2022 ASH Annual Meeting, evaluating Venetoclax plus hypomethylating agents in young adults with newly diagnosed AML and adverse ELN risk, showed a complete remission with incomplete hematologic recovery (CRc) rate of 78% after one cycle of treatment, with a minimal residual disease (MRD) negativity rate of 77%. After two cycles of treatment, the CRc rate was 91.9% with an MRD negativity rate of 82.3%. The CRc rates for favorable, intermediate, and adverse risk groups were 69.6%, 75.4%, and 61.3%, respectively. Although the combination of Venetoclax and demethylating agents has shown promising efficacy, there are still limitations such as adverse events including thrombocytopenia (46%), nausea (44%), constipation (43%), neutropenia (42%), febrile neutropenia (42%), diarrhea (41%), and tumor lysis syndrome (TLS), as well as suboptimal achievement of MRD negativity and depth of remission after induction therapy.
Granulocyte colony-stimulating factor (G-CSF) is expressed by almost all AML cells and binds to its receptor, G-CSFR. In pre-activation regimens, G-CSF induces tumor cells in the quiescent phase (G0/G1) to enter the proliferative phase (S phase), enhancing the cytotoxic effect of chemotherapy drugs on tumor cells, improving the efficacy of chemotherapy, and reducing adverse reactions. A study conducted by Tang Xiaowen's team at the First Affiliated Hospital of Soochow University on the efficacy and safety of decitabine (DAC) combined with HAAG in the treatment of newly diagnosed acute myeloid leukemia showed that after one cycle of DAC+HAAG induction therapy in 50 patients, 48 patients (96%) achieved complete remission (CR)/CR with incomplete blood count recovery (CRp)/CR with incomplete count recovery and incomplete marrow recovery (CRi), and 2 patients (4%) achieved partial remission (PR). The median time to recovery of white blood cell count, platelet count, and hemoglobin was 17.5 days, 19.0 days, and 20.0 days, respectively. Only 16% (8/50) and 6% (3/50) of patients experienced grade 3-4 infections and bleeding, while non-hematologic toxicities were mainly grade 1-2 and resolved after symptomatic treatment.
The combination of venetoclax and hypomethylating agents is the most common approach, which synergistically induces cell apoptosis and reduces MCL-1 levels, thereby overcoming resistance to BCL-2 inhibitors. Additionally, the combination interferes with the energy metabolism of leukemia cells and targets leukemia stem cells. However, there is currently no research on the combination of azacitidine, venetoclax, and G-CSF. The investigators has conducted a preliminary clinical study on the VAG regimen (azacitidine, venetoclax, and granulocyte colony-stimulating factor) for newly diagnosed AML, which has shown promising results. We plan to expand the sample size and further investigate its mechanism of tumor cell killing.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| VAG regimen in the treatment of newly diagnosed acute myeloid leukemia (AML) | Experimental | Drug: Venetoclax 100 mg d1,200 mg d2,400 mg d3-28;AZA: 75mg/m2 on days 1-7 VEN: 100mg on day 1, 200mg on day 2, 400mg on days 3-28 G-CSF: 50-600ug/day, starting on day 1 (adjusted based on WBC count of 10-25*10E9/L) In the induction phase of the ND-AML treatment protocol, VEN+AZA+G-CSF is administered. At the end of the induction phase, the efficacy is evaluated. If the patient achieves complete remission (CR), the original treatment protocol is continued for consolidation. If the patient achieves partial remission (PR), the original treatment protocol is repeated for induction until the patient achieves CR or shows no response (NR), progressive disease (PD), or relapse (PR/NR/PD). If the patient shows no response or progressive disease, the study is concluded. |
Who may qualify
- Ages
- 18 to 75 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- Age between 18 and 75 years, regardless of gender.
- Diagnosis of AML (excluding APL) according to the 2022 World Health Organization (WHO) diagnostic criteria.
- ECOG performance status of 0-2.
- For female participants of childbearing potential or male participants with female partners of childbearing potential, effective contraceptive measures must be taken throughout the entire treatment period and for 6 months after the treatment period.
- Expected survival of at least 3 months.
Key exclusion criteria (9 listed)
- Acute promyelocytic leukemia (M3 subtype).
- Central nervous system leukemia.
- Severe uncontrolled infection or other major diseases.
- Heart failure: Ejection fraction (EF) < 50%, New York Heart Association (NYHA) class II or above.
- Impaired liver or kidney function: Serum total bilirubin ≥ 2.0 mg/dl, AST ≥ 3 times the upper limit of normal, serum creatinine clearance rate (Ccr) ≥ 50 ml/min, arterial oxygen saturation (SpO2) < 92%.
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 |
|---|---|---|
| Venetoclax 100 mg d1,200 mg d2,400 mg d3-28;Also: AZA 75mg/m2 on days 1-7, G-CSF: 50-600ug/day, starting on day 1 (adjusted based on WBC count of 10-25*10E9/L)VAG in the induction phase of the ND-AML treatment protocol | Drug | VAG regimen in the treatment of newly diagnosed acute myeloid leukemia (AML) |
Primary outcome
Complete Remission (CR)
Time frame: The period of 2 months from the start of treatment.
A. No symptoms or signs of leukemia cell infiltration, normal or near-normal life; B. Blood counts: Hb ≥ 100g/L (males) or ≥ 90g/L (females and children), absolute neutrophil count ≥ 1.5 × 109/L, platelets ≥ 100 × 109/L. No leukemia cells in peripheral blood leukocyte classification; C. Bone marrow morphology: Less than or equal to 5% of myeloblasts (type I + type II) (primitive monocytes + immature monocytes or primitive lymphocytes + immature lymphocytes), normal red blood cells and megakaryocytes; D. No extramedullary leukemia (no lymphadenopathy, splenomegaly, skin/gum infiltration, testicular masses, central nervous system involvement).
5 secondary outcomes
Partial Remission (PR)
Time frame: The period of 1 month from the start of treatment.
Complete Remission with incomplete blood count recovery (CRi)
Time frame: The period of 1 month from the start of treatment.
Overall Response Rate (ORR)
Time frame: The period of 4 months from the start of treatment.
Morphologic leukemia-free state (MLFS)
Time frame: The period of 1 month from the start of treatment.
Overall survival, OS
Time frame: The period of 2 years from the start of treatment.
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Aug 2024.
- 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.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Venetoclax 100 mg d1,200 mg d2,400 mg d3-28; in people with Acute Myeloid Leukemia, run by Yang Xiaotian at 1 site in China.
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 6 inclusion and 9 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: looking for participants now, as of the sponsor's last update on 2 Aug 2024. 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 China. 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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Xiaotian Yang (15695110492, 15695110492@163.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Complete Remission (CR) (time frame: The period of 2 months from the start of treatment.). 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 2 Aug 2024.