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New treatment option for Lymphoma
Official title AZD3470 as Monotherapy or in Combination With Anticancer Agent(s) in Participants With Haematologic Malignancies.
ClinicalTrials.gov ID: NCT06137144
What this study is testing
What is AZD3470?
AZD3470 is an investigational medicine, given as an infusion into a vein, being studied as a potential treatment for lymphoma.
Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.
- What it's testing
- This study is designed to evaluate the safety, tolerability, PK, pharmacodynamics, and preliminary efficacy following oral administration of AZD3470 as a monotherapy, and in combination with other anticancer agents in participants with haematologic malignancies.
- Phase 2: a mid-size study of how well it works
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 12 and older
You may be able to join if
- Core
- Adequate adult (ECOG) or adolescent (Karnofsy or Lanksy) Performance Score assessments
- Adequate organ and bone marrow function. Module 1 Cohort 1:
- Age:
- Part A (dose escalation): aged ≥ 18 years at the time of signing the informed consent.
You likely can't join if
- Core Exclusion criteria:
- Any significant laboratory finding or any severe and uncontrolled medical condition.
- Active CNS involvement by lymphoma, leptomeningeal disease, or spinal cord compression.
- Serologic active HBV or HCV infection.
- Known to have tested positive for HIV.
- Active gastrointestinal disease or other condition that will interfere with oral therapy.
See the full eligibility criteria
Who can join
- Core
- Adequate adult (ECOG) or adolescent (Karnofsy or Lanksy) Performance Score assessments
- Adequate organ and bone marrow function. Module 1 Cohort 1:
- Age:
- Part A (dose escalation): aged ≥ 18 years at the time of signing the informed consent.
- Part B (optimization): aged ≥ 12 years of age. Adolescent participants must weigh ≥ 40 kg.
- Histologically confirmed diagnosis of cHL based on WHO criteria
- Previous treatment with at least 2 prior lines of therapy for the treatment of cHL (including at least 2 cycles of BV and anti-PD1) and have documented r/r active disease requiring treatment.
- Participants must provide FFPE baseline tumour tissue.
- At least 1 radiographically measurable, and/or FDG-avid lymphoma lesion ( \>1.5 cm for nodal lesion and \>1 cm for extranodal lesion). Module 1 Cohort 2:
- Participants must be at least 50 years of age or older at study entry.
- Histologically confirmed diagnosis of cHL based on WHO criteria
- Ann Arbor stages III or IV.
- Participant must have previously received at least 4 cycles of SoC combination therapy with A-AVD, N-AVD, AVD, or ABVD (based on regional SOC, per investigator) as finite first-line induction therapy, and achieved at...
- Participants must provide FFPE baseline tumour tissue. Module 1 Cohort 3:
- Participants must be aged ≥ 18 years at the time of signing the informed consent.
- Histologically confirmed diagnosis of PTCL NOS, systemic ALCL, or AITL based on WHO criteria.
- Participants must have received at least 1 prior line of therapy for the treatment of PTCL and have exhausted all available therapies with demonstrated clinical benefit. Participants with ALCL must have received prior...
- Participants must provide FFPE baseline tumour tissue a. Ability to provide an on-treatment biopsy (if the tumour is suitable for biopsy).
- At least 1 radiographically measurable, and/or FDG-avid lymphoma lesions (\> 1.5 cm for nodal lesion and \>1 cm for extranodal lesion). Module 2 Cohort 1:
- Participants must be aged ≥ 18 years at the time of signing the informed consent.
- Histologically confirmed diagnosis of cHL based on WHO criteria
- At least 1 radiographically measurable, and/or FDG-avid lymphoma lesions (\> 1.5 cm for nodal lesion and \>1 cm for extranodal lesion).
- Participant must have received at least 1 prior line of therapy for the treatment of cHL and have documented r/r active disease requiring treatment.
- Participants must provide FFPE baseline tumour tissue.
What rules you out
- Core Exclusion criteria:
- Any significant laboratory finding or any severe and uncontrolled medical condition.
- Active CNS involvement by lymphoma, leptomeningeal disease, or spinal cord compression.
- Serologic active HBV or HCV infection.
- Known to have tested positive for HIV.
- Active gastrointestinal disease or other condition that will interfere with oral therapy.
- Any of the following ECG cardiac criteria: Mean resting QTcF \> 470 msec, clinically important abnormalities in rhythm, conduction or morphology, and/or any factors that increase the risk of QTc prolongation or risk of...
- Undergone any of the following procedures within 6 months prior to first dose:
- Coronary artery bypass graft,
- Percutaneous coronary intervention or heart valve replacement or repairment,
- Vascular stent implantation (venous stent is eligible),
- Acute coronary syndrome / myocardial infarction,
- Unstable or poorly controlled angina pectoris,
- Ventricular arrhythmias requiring continuous therapy,
- Uncontrolled atrial fibrillation,
- Haemorrhagic or thrombotic stroke (including transient ischaemic attacks) or any other CNS bleeding.
- Acute venous or atrial thromboembolic event (unless considered stable or adequately treated with at least 3months of therapeutic anticoagulation).
- Severe valvular heart disease.
- Congestive heart failure Grade II to Grade IV.
- Prior or current cardiomyopathy.
- Uncontrolled hypertension.
- History of significant haemoptysis or haemorrhage within4 weeks of the first dose of study treatment.
- Unresolved toxicities of Grade \> 1 from prior anti cancer therapy (excluding peripheral neuropathy, vitiligo, alopecia and endocrine disorders that are controlled with replacement hormone therapy, and asymptomatic...
- History of another primary malignancy.
- Received the following anticancer therapies: anti-lymphoma therapy (within 21 days), radiation therapy(within 28 days), allo-HSCT (within 180 days), auto-HSCT/cellular therapy (within 60 days), or MAT2A or PRMT5...
- Requires ongoing immunosuppressive therapy, including systemic corticosteroids. Module 2 Cohort 1:
- History of confirmed ILD, drug-induced ILD, radiation pneumonitis requiring steroid treatment or any evidence of clinically active ILD or pneumonitis.
- ≥Grade 3 immune-mediated AE while receiving prior checkpoint inhibitor immunotherapy, or any unresolved ≥Grade 2 immune-mediated AE.
- History of immune-mediated myocarditis or pericarditis.
- Experienced a toxicity that led to permanent discontinuation of prior immunotherapy.
- Active or prior documented pathologically confirmed autoimmune or inflammatory disorders
- Refractory to prior checkpoint inhibitor therapy (within 12 weeks of last dose)
- Eligible for allogeneic or autologous stem cell transplant.
- Received an allogeneic HSCT within 5 years of the first dose of study treatment; must not have active Graft-versus-host disease.
- Participants with a known hypersensitivity to pembrolizumab or any of the excipients of the product.
The study team makes the final eligibility decision.
Where it's taking place
- Duarte, California, United States
- Miami, Florida, United States
- Atlanta, Georgia, United States
- Boston, Massachusetts, United States
- New York, New York, United States
- Philadelphia, Pennsylvania, United States
- Houston, Texas, United States
- Adelaide, Australia
- Birtinya, Australia
- Fitzroy, Australia
- Nedlands, Australia
- South Brisbane, Australia
- Waratah, Australia
- Beijing, China
- Guangzhou, China
- Shanghai, China
- Créteil, France
- Dijon, France
- Lille, France
- Pierre-Bénite, France
+ 15 more site(s).
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 12 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Duarte, California, United States; Miami, Florida, United States; Atlanta, Georgia, United States; Boston, Massachusetts, United States; New York, New York, United States; Philadelphia, Pennsylvania, United States and 29 more location(s). Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.