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RecruitingNCT05906862Updated Aug 14, 2025

AMT-253 in Patients With Selected Advanced Solid Tumours

A Phase 1 interventional study of AMT-253 in Advanced Solid Tumor, sponsored by Multitude Therapeutics (Australia) Pty Ltd. Recruiting at 7 sites in Australia. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-08-14.

Sponsored by Multitude Therapeutics (Australia) Pty Ltd · Phase 1, Interventional, and Treatment

From the registry’s dates

  • Started Nov 2023; still recruiting 2 years 11 months later.
Phase
Phase 1
Study type
Interventional
Enrollment
54
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

This first-in-human study will evaluate the Maximum Tolerated Dose (MTD) / the Recommended Phase 2 Dose (RP2D), safety, tolerability, anti-tumor activity, pharmacokinetics, pharmacodynamics and immunogenicity of AMT-253, in Patients with Advanced Solid Tumors

02

Conditions studied

  • Advanced Solid Tumor
03

In context

Lead sponsor

Multitude Therapeutics (Australia) Pty Ltd is the lead sponsor of 2 studies on the registry; 2 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

Eligibility criteria

Key Inclusion Criteria:

  • Patients must be willing and able to sign the ICF, and to adhere to the study visit schedule and other protocol requirements.
  • Age ≥18 years (at the time consent is obtained).
  • Patients who have undergone at least one systemic therapy and have radiologically or clinically determined progressive disease during or after most recent line of therapy, and for whom no further standard therapy is available, or who are intolerable to standard therapy.
  • Patients must have at least one measurable lesion as per RECIST version 1.1
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.
  • Life expectancy ≥ 3 months.
  • Patients must have adequate organ function.
  • Women of child bearing potential (WCBP), defined as a sexually mature woman who has not undergone surgical sterilization or who has not been naturally postmenopausal for at least 12 consecutive months (i.e., who has had menses any time in the preceding 12 consecutive months) must agree to use two effective contraceptive methods (examples include oral, parenteral, or implantable hormonal contraceptive, intra-uterine device, barrier contraceptive with spermicide, partner's latex condom or vasectomy) while on study treatment and for at least twelve weeks after the last dose of the IMP.
  • WCBP must have a negative serum pregnancy test within 7 days prior to first dose of the IMP.
  • Male patients must agree to use a latex condom, even if they had a successful vasectomy, while on study treatment and for at least twelve weeks after the last dose of the IMP.
  • Male patients must agree not to donate sperm, and female patients must agree not to donate eggs, while on study treatment and for at least 12 weeks after the last dose of the IMP.
  • Availability of tumor tissue sample (either an archival specimen or a fresh biopsy material) at screening.

Key Exclusion Criteria:

  • Central nervous system (CNS) metastasis.
  • Active or chronic skin disorder requiring systemic therapy.
  • History of Steven's Johnson's syndrome or toxic epidermal necrolysis syndrome.
  • Active ocular conditions requiring treatment or close monitoring, including, but not limited to: macular degeneration, papilledema, active diabetic retinopathy with macular oedema, wet age-related macular degeneration requiring intravitreal injections, or uncontrolled glaucoma.
  • Persistent toxicities from previous systemic anti-neoplastic treatments of Grade >1.
  • Systemic anti-neoplastic therapy within five half-lives or 21 days, whichever is shorter, prior to first dose of the IMP.
  • Radiotherapy to lung field at a total radiation dose of ≥20 Gy within 6 months, wide-field radiotherapy (e.g., > 30% of marrow-bearing bones) within 28 days.
  • Major surgery (not including placement of vascular access device or tumor biopsies) within 28 days prior to first dose of the IMP, or no recovery from side effects of such intervention.
  • Significant cardiac disease, such as recent (within six months prior to first dose of the IMP) myocardial infarction or acute coronary syndromes (including unstable angina pectoris), congestive heart failure (New York Heart Association class III or IV), uncontrolled hypertension, uncontrolled cardiac arrhythmias.
  • Has a history of (non-infectious) interstitial lung disease (ILD)/pneumonitis that required steroids, or current ILD/pneumonitis, or suspected ILD/pneumonitis (e.g., idiopathic pulmonary fibrosis, organizing pneumonia, drug-induced pneumonitis, idiopathic pneumonitis, etc.).
  • History of thromboembolic or cerebrovascular events, including transient ischemic attacks, cerebrovascular accidents, deep vein thrombosis, or pulmonary emboli within six months prior to first dose of the IMP.
  • Acute and/or clinically significant bacterial, fungal or viral infection including hepatitis B (HBV), hepatitis C (HCV), known human immunodeficiency virus (HIV).
  • Administration of a live vaccine within 28 days prior to the administration of the first dose of the IMP.
  • Patients requiring concurrent treatment of strong inhibitors or inducers of cytochrome P450 3A4 or 1A2 enzyme (CYP3A4 or CYP1A2) within 2 weeks prior to the first dose and during the study treatment.
  • Patient who has active graft versus host disease, or diagnosis of immunodeficiency, or has an active autoimmune disease or other conditions that require systemic steroid therapy, i.e. > 10 mg daily prednisone equivalents within 14 days prior to the administration of the first dose; the use of short-course systemic corticosteroids (≤ 7 days) is permitted, with a wash-out period of 1 week prior to the administration of the first dose of the IMP.
  • Known or suspected severe allergy/hypersensitivity (resulting in treatment discontinuation) to monoclonal antibodies.
  • Known or suspected intolerance to the components of the IMP.
  • Concurrent participation in another investigational therapeutic clinical trial.
  • Patients with known active alcohol or drug abuse.
  • Pregnant or breast-feeding females.
  • Mental or medical conditions that prevent the patient from giving informed consent or complying with the trial or other severe acute or chronic medical or psychiatric conditions or laboratory abnormality that may increase the risk associated with the study participation or the IMP administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the patient inappropriate for enrolment in this study.
  • Prior history of malignancy other than inclusion diagnosis within five years prior to first dose of the IMP.

Note: Other protocol defined Inclusion/Exclusion criteria apply.

05

Study design

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

Study arms

  • Experimental
    AMT-253 Dose Escalation

    Drug: AMT-253

Interventions

  • DrugAMT-253

    Administered intravenously

06

What researchers measure

Primary outcomes

  1. Recommended Phase 2 Dose (RP2D)

    The RP2D will be determined using dose limiting toxicities (DLTs) and all other available study data

    Time frame: Up to 24 months

  2. Maximum Tolerated Dose (MTD)

    The MTD will be determined using DLTs

    Time frame: Up to 24 months

  3. Type, incidence and severity of Adverse Events

    Safety and tolerability profile assessed by the Common Terminology Criteria for Adverse Events v5.0

    Time frame: Up to 24 months

Secondary outcomes

  1. Overall Response Rate (ORR) according to the Response Evaluation Criteria in Solid Tumors (RECIST) v1.1

    Proportion of patients achieving Complete Response (CR) or Partial Response (PR)

    Time frame: Up to 24 months

  2. Disease Control Rate (DCR) according to the RECIST v1.1

    Proportion of patients achieving CR, PR or Stable Disease (SD)

    Time frame: Up to 24 months

  3. Progression-free Survival (PFS)

    Time from date of start of treatment to date of the first progression or death, whichever occurs first.

    Time frame: Up to 24 months

  4. Concentration of anti-drug antibodies (ADA)

    Immunogenicity profile characterized by concentration of ADAs

    Time frame: Up to 24 months

  5. Maximum observed concentration (C[max])

    Pharmacokinetic profile characterized by the maximum observed concentration (C\[max\]) of AMT-253

    Time frame: Up to 24 months

  6. Area under the curve (AUC)

    Pharmacokinetic profile characterized by the area under the curve (AUC) of AMT-253

    Time frame: Up to 24 months

  7. Terminal half-life (t[1/2])

    Pharmacokinetic profile characterized by the terminal half-life (t\[1/2\]) of AMT-253

    Time frame: Up to 24 months

  8. Time to maximum concentration (Tmax)

    Pharmacokinetic profile characterized by the time to maximum concentration (Tmax) of AMT-253

    Time frame: Up to 24 months

07

Study locations

7 of 7 sites recruiting
  • Blacktown
    Sydney, New South Wales, Australia
    • Gao Bo · Contact
    Recruiting
  • Chris O'Brien Lifehouse
    Sydney, New South Wales, Australia
    • Steven Kao · Contact · 61 02 8514 0140
    Recruiting
  • Maquarie University Hospital
    Sydney, New South Wales, Australia
    • John Park · Contact
    Recruiting
  • ICON Cancer Centre
    Brisbane, Queensland, Australia
    • Jermaine Coward · Contact
    Recruiting
  • Southern Oncology Clinical Research
    Adelaide, South Australia, Australia
    • Ganessan Kichenadasse · Contact
    Recruiting
  • Cabrini Malvern Hospital
    Malvern, Victoria, Australia
    • Richardson Gary · Contact · 61 03 9508 9542
    Recruiting
  • Alfred Hospital
    Melbourne, Victoria VIC 3004, Australia
    • Mark Voskoboynik · Contact
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 14, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05906862
Lead sponsor
Multitude Therapeutics (Australia) Pty Ltd
Responsible party
Sponsor
First posted
Jun 18, 2023
Start date
Nov 6, 2023
Primary completion
Sep 30, 2026 (estimated)
Completion
Dec 30, 2026 (estimated)
Last update
Aug 14, 2025

Study contacts

Jane Zhu
Contact
juanjuan.zhu@multitudetherapeutics.com
13917933915

Oversight

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

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