A Phase 1 interventional study of AWT020 in Advanced Cancers (Solid Tumors), sponsored by Anwita Biosciences. Recruiting at 2 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-23.
Sponsored by Anwita Biosciences · Phase 1, Interventional, and Treatment
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This study is aimed at establishing the MTD and/or the RP2D for AWT020 monotherapy and to provide safety, tolerability, efficacy, PK, immunogenicity characteristics of AWT020.
This study will enroll participants who have undergone at least one systemic therapy and have progressive disease during or after most recent line of therapy, and for whom no further standard therapy (that is known to confer clinical benefit) is available, or who are intolerant of standard therapy. The study design consists of two parts: dose escalation (BOIN design) and dose optimization. Participants enrolled into this study will be assigned to one of 4 dose levels and will receive AWT020 via intravenous infusion at a regular interval. The treatment will be continued until disease progression, withdrawal from study or death. The primary objective is to investigate the safety of this agent. The secondary objective is to investigate the pharmacokinetics, pharmacodynamic, potential anti-tumor activity and immunogenicity of this agent.
Anwita Biosciences is the lead sponsor of 3 studies on the registry; 3 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
The diagnosis was confirmed by looking at a sample under a microscope: tissue from a biopsy or surgery (histology), or cells from a fluid or needle sample (cytology).
Your pathology report is the document that shows this.
The amount of disease can be tracked with a defined measurement, so the study can see whether it shrinks or grows. It might be a tumour measured on a scan or, in some blood cancers such as myeloma, a marker measured in blood or urine.
The criteria or the study team say which measurement counts — having no tumour visible on a scan does not by itself rule you out.
The standard rules for measuring tumours on CT or MRI scans, to tell whether a cancer is shrinking, stable or growing during treatment.
“Measurable disease per RECIST 1.1” usually means at least one tumour 10 mm or more at its longest on a CT scan, or a lymph node 15 mm or more across its short axis.
A scale of how much an illness limits everyday activity. For people being assessed to join a study, scores run from 0 (fully active) to 4; lower is more active.
Studies most often ask for 0–1 or 0–2. Your doctor gives the score; the WHO scale uses the same steps. The full scale also has 5, which records death.
The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.
An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.
Cancer that has spread from where it began to other parts of the body. “Metastatic” cancer is cancer that has spread this way.
Cancer that has spread to the leptomeninges, the thin layers covering the brain and spinal cord, and the fluid between them. It is not the same as brain metastases.
Criteria often treat it separately, and many studies leave it out even where treated brain metastases are allowed.
Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.
A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.
Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.
Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.
Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.
Vaccines made with a weakened form of the germ, such as measles–mumps–rubella (MMR), chickenpox and yellow fever. They can be risky when the immune system is weakened. Flu injections are not live; the nasal flu spray is.
A planned gap after a treatment, so that its effects can lessen before the study treatment or a study assessment. Ask the study team and the doctor who prescribed it before changing any medicine.
Stem cell (bone marrow) transplants. Allogeneic uses cells from a donor; autologous uses your own cells, collected earlier and given back.
A drug or device being studied in a clinical trial.
It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.
Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.
Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.
Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Histologically or cytologically confirmed
The diagnosis was confirmed by looking at a sample under a microscope: tissue from a biopsy or surgery (histology), or cells from a fluid or needle sample (cytology).
Your pathology report is the document that shows this.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Measurable disease
The amount of disease can be tracked with a defined measurement, so the study can see whether it shrinks or grows. It might be a tumour measured on a scan or, in some blood cancers such as myeloma, a marker measured in blood or urine.
The criteria or the study team say which measurement counts — having no tumour visible on a scan does not by itself rule you out.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
RECIST
The standard rules for measuring tumours on CT or MRI scans, to tell whether a cancer is shrinking, stable or growing during treatment.
“Measurable disease per RECIST 1.1” usually means at least one tumour 10 mm or more at its longest on a CT scan, or a lymph node 15 mm or more across its short axis.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
ECOG performance status
A scale of how much an illness limits everyday activity. For people being assessed to join a study, scores run from 0 (fully active) to 4; lower is more active.
Studies most often ask for 0–1 or 0–2. Your doctor gives the score; the WHO scale uses the same steps. The full scale also has 5, which records death.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Life expectancy
The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Hypersensitivity
An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Metastases
Cancer that has spread from where it began to other parts of the body. “Metastatic” cancer is cancer that has spread this way.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Leptomeningeal disease
Cancer that has spread to the leptomeninges, the thin layers covering the brain and spinal cord, and the fluid between them. It is not the same as brain metastases.
Criteria often treat it separately, and many studies leave it out even where treated brain metastases are allowed.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Clinically significant
Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Autoimmune disease
A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.
Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Corticosteroids (steroids)
Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.
Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Live vaccines
Vaccines made with a weakened form of the germ, such as measles–mumps–rubella (MMR), chickenpox and yellow fever. They can be risky when the immune system is weakened. Flu injections are not live; the nasal flu spray is.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Washout period
A planned gap after a treatment, so that its effects can lessen before the study treatment or a study assessment. Ask the study team and the doctor who prescribed it before changing any medicine.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Allogeneic and autologous transplant
Stem cell (bone marrow) transplants. Allogeneic uses cells from a donor; autologous uses your own cells, collected earlier and given back.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Investigational drug or device
A drug or device being studied in a clinical trial.
It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Cancer (malignancy)
Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.
Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Participants receiving intravenous infusion of AWT020
Biological: AWT020
Participants receiving AWT020 once every three weeks at designated dose levels
Adverse Events (AEs) [Safety]
Type, incidence, and severity of Adverse Events (AEs)
Time frame: Throughout the study up to 30 months
Serious Adverse Events (SAEs) [Safety]
Type, incidence, and severity of Serious Adverse Events (SAEs)
Time frame: Throughout the study up to 30 months
Treatment-emergent Adverse Events (TEAEs) [Safety]
Type, incidence, and severity of treatment-emergent adverse events (TEAEs)
Time frame: Throughout the study up to 30 months
Adverse Events of Special Interest (AESIs) [Safety]
Type, incidence, and severity of adverse events of special interest (AESIs)
Time frame: Throughout the study up to 30 months
Dose-limiting Toxicities (DLTs) [Tolerability]
Incidence of dose-limiting toxicity (DLT)
Time frame: Throughout the study up to 30 months
Maximum Observed Serum Concentration (Cmax)
Blood samples will be collected to characterize the pharmacokinetics (PK) of AWT020
Time frame: Throughout the study up to 30 months
Time to Cmax (Tmax)
Blood samples will be collected to characterize the pharmacokinetics (PK) of AWT020
Time frame: Throughout study up to 30 months
Area Under the Curve (AUC)
Blood samples will be collected to characterize the pharmacokinetics (PK) of AWT020
Time frame: Throughout the study up to 30 months
Clearance (CL)
Blood samples will be collected to characterize the pharmacokinetics (PK) of AWT020
Time frame: Throughout the study up to 30 months
Volume of Distribution (Vss)
Blood samples will be collected to characterize the pharmacokinetics (PK) of AWT020
Time frame: Throughout the study up to 30 months
Half-life (t1/2)
Blood samples will be collected to characterize the pharmacokinetics (PK) of AWT020
Time frame: Throughout the study up to 30 months
Overall Response Rate (ORR)
Overall response rate (ORR) assessed by the Investigator according to the Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1
Time frame: Throughout study up to 30 months
Disease Control Rate (DCR)
Disease control rate (DCR) assessed by the Investigator according to the Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1
Time frame: Throughout the study up to 30 months
Progression-free Survival (PFS)
Time to response and duration of response assessed by the Investigator according to RECIST version 1.1
Time frame: Throughout the study up to 30 months
Immune-related ORR (iORR)
Immune-related overall response rate (iORR) assessed by the Investigator according to immune RECIST (iRECIST)
Time frame: Throughout the study up to 30 months
Immune-related DCR (iDCR)
Immune-related disease control rate (iDCR) assessed by the Investigator according to immune RECIST (iRECIST)
Time frame: Throughout the study up to 30 months
Immune-related PFS (iPFS)
Immune-related progression-free survival (iPFS) assessed by the Investigator according to iRECIST
Time frame: Throughout the study up to 30 months
Immune-related TTR (iTTR)
Immune-related time to response (iTTR) assessed by the Investigator according to iRECIST
Time frame: Throughout the study up to 30 months
Immune-related DOR (iDOR)
Immune-related duration of response (iDOR) assessed by the Investigator according to iRECIST
Time frame: Throughout the study up to 30 months
Overall Survival
The time from first dose of study treatment to death from any cause
Time frame: Throughout study up to 30 months
Immunogenicity of AWT020
Incidence of anti-drug antibodies (ADAs)
Time frame: Throughout study up to 30 months
Serum Cytokine Concentrations
Blood samples will be collected to characterize the pharmacodynamics (PD) of AWT020
Time frame: Throughout study up to 30 months
T-cell Activation Markers
Blood samples will be collected to characterize the pharmacodynamics (PD) of AWT020
Time frame: Throughout the study up to 30 months
PD-L1 Expression
Assessment of PD-L1 expression level in tumor tissue samples
Time frame: Throughout the study up to 30 months
Tumor-infiltrating Immune Cell Populations
Assessment of tumor-infiltrating immune cell populations in tumor tissue samples
Time frame: Throughout the study up to 30 months
Plan to share: No
No publications or documents are linked to this record.
Start is estimated for Sep 2026; primary completion for Jan 2029, 28 months later.
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Studies of the drug tested here: Alpha-PD1/IL2 Fusion Protein AWT020
Anwita Biosciences