ClinicalTrials.gg
RecruitingNCT07822919Updated Sep 23, 2026

A Study of AWT020 in Participants With Advanced Solid Tumors

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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Phase
Phase 1
Study type
Interventional
Enrollment
96
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Advanced Cancers (Solid Tumors)

Keywords

  • AWT020
  • anti-PD1
  • Interleukine-2
  • Phase 1
03

In context

Lead sponsor

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.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

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.

Inclusion criteria

  • Age 18 years or older; able to provide written and comply with study visits and procedures.
  • confirmed, unresectable advanced solid tumor.
  • Disease progression after at least one systemic therapy, with no beneficial standard option available or tolerated. Disease-specific prior therapy requirements apply to urothelial and renal cell carcinoma cohorts.
  • At least one by version 1.1, performance status of 0 or 1, and of at least 3 months.
  • Adequate bone marrow, renal, hepatic, coagulation, and cardiac function as defined in the protocol.
  • Meets protocol requirements for reproductive safety and tumor tissue availability.

Exclusion criteria

Exclusion Criteria:

  • Relevant or intolerance to prior immunotherapy, interleukin-2 based therapy, monoclonal antibodies, or the study treatment; or prior immunotherapy discontinued because of an immune-related adverse event.
  • Untreated or unstable central nervous system , , or brainstem metastases.
  • or skin disease requiring systemic treatment; Stevens-Johnson syndrome or toxic epidermal necrolysis; or current, suspected, or -treated interstitial lung disease/pneumonitis.
  • Unresolved toxicity from prior therapy, or recent anticancer treatment, major surgery, , or other restricted therapy within protocol-defined .
  • Clinically significant cardiac, thromboembolic, cerebrovascular, gastrointestinal, bleeding, or other uncontrolled medical condition.
  • Active or recent severe infection.
  • Prior transplantation or adoptive cellular immunotherapy; concurrent therapeutic trial; or pregnancy or breastfeeding.
  • Another within 5 years, except permitted low-risk or in situ cancers; or any condition that increases risk, prevents consent or compliance, or could interfere with study interpretation.
Terms in these criteria, in plain language(17)

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.

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.

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.

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.

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.

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.

0
Fully active, no restrictions.
1
Limited in strenuous activity, but walking and able to do light work, such as housework or office work.
2
Walking and able to look after yourself, but unable to work; up and about more than half of waking hours.
3
Able to look after yourself only in part; in bed or a chair more than half of waking hours.
4
Unable to look after yourself at all; in bed or a chair all day.

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.

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.

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.

Metastases

Cancer that has spread from where it began to other parts of the body. “Metastatic” cancer is cancer that has spread this way.

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.

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.

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.

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.

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.

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.

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.

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.

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.

05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
96 participants (estimated)

Study arms

  • Experimental
    AWT020

    Participants receiving intravenous infusion of AWT020

    Biological: AWT020

Interventions

  • BiologicalAWT020

    Participants receiving AWT020 once every three weeks at designated dose levels

06

What researchers measure

Primary outcomes

  1. Adverse Events (AEs) [Safety]

    Type, incidence, and severity of Adverse Events (AEs)

    Time frame: Throughout the study up to 30 months

  2. Serious Adverse Events (SAEs) [Safety]

    Type, incidence, and severity of Serious Adverse Events (SAEs)

    Time frame: Throughout the study up to 30 months

  3. 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

  4. 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

  5. Dose-limiting Toxicities (DLTs) [Tolerability]

    Incidence of dose-limiting toxicity (DLT)

    Time frame: Throughout the study up to 30 months

Secondary outcomes

  1. 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

  2. Time to Cmax (Tmax)

    Blood samples will be collected to characterize the pharmacokinetics (PK) of AWT020

    Time frame: Throughout study up to 30 months

  3. 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

  4. Clearance (CL)

    Blood samples will be collected to characterize the pharmacokinetics (PK) of AWT020

    Time frame: Throughout the study up to 30 months

  5. 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

  6. 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

  7. 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

  8. 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

  9. 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

  10. 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

  11. 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

  12. 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

  13. 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

  14. 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

  15. Overall Survival

    The time from first dose of study treatment to death from any cause

    Time frame: Throughout study up to 30 months

  16. Immunogenicity of AWT020

    Incidence of anti-drug antibodies (ADAs)

    Time frame: Throughout study up to 30 months

Other outcomes

  1. Serum Cytokine Concentrations

    Blood samples will be collected to characterize the pharmacodynamics (PD) of AWT020

    Time frame: Throughout study up to 30 months

  2. 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

  3. PD-L1 Expression

    Assessment of PD-L1 expression level in tumor tissue samples

    Time frame: Throughout the study up to 30 months

  4. 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

07

Study locations

2 of 2 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Sep 2026; primary completion for Jan 2029, 28 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 2, 2026
First posted
Sep 16, 2026
StartEst.
Sep 11, 2026
Primary completionEst.
Jan 2029
CompletionEst.
Feb 2029
Last update
Sep 23, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 23, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07822919
Lead sponsor
Anwita Biosciences
Responsible party
Sponsor
First posted
Sep 16, 2026
Start date
Sep 11, 2026 (estimated)
Primary completion
Jan 2029 (estimated)
Completion
Feb 2029 (estimated)
Last update
Sep 23, 2026

Study contacts

Laksmi Wilson
Contact
lwilson@anwitabio.com
650-600-9828
Harshad Amin, MD
principal investigator · Florida Clinical Trials Group

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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Studies of the drug tested here: Alpha-PD1/IL2 Fusion Protein AWT020

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