ClinicalTrials.gg
RecruitingNCT06440005Updated Sep 9, 2026

A Study to Evaluate Safety, Tolerability and Preliminary Activity of AGX101 in Participants With Advanced Solid Tumors

A Phase 1 interventional study of AGX101 in Cancer, Advanced Cancer and Locally Advanced Carcinoma, sponsored by Angiex, Inc.. Recruiting at 7 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-09.

Sponsored by Angiex, Inc. · Phase 1, Interventional, and Treatment

From the registry’s dates

  • Started Jul 2024; still recruiting 2 years 3 months later.
Phase
Phase 1
Study type
Interventional
Enrollment
80
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

AGX101 is an antibody-drug conjugate (ADC) therapy for tumor-forming cancers. The purpose of this study is to learn about AGX101 effects and safety at various dose levels in an all-comers advanced solid cancer patient population. AGX101will be administered intravenously.

Dosing of AGX101 will be repeated once every 3, 6 or 9 weeks. Participants may continue study treatment until disease progression, unacceptable toxicity, or consent withdrawal. Subjects will attend an end of treatment visit and will receive two safety follow-up telephone contacts up to 90 days following the last dose of study drug.

02

Conditions studied

  • Cancer
  • Advanced Cancer
  • Locally Advanced Carcinoma
  • Metastatic Solid Tumor
  • Breast Cancer
  • Prostate Cancer
  • Colorectal Cancer
  • Pancreatic Cancer
  • Liver Cancer
  • Angiosarcoma
  • Solid Tumor

Keywords

  • ADC
  • Antibody Drug Conjugate
  • AGX101
03

In context

Neoplasms

10,818 studies on the registry are indexed under Neoplasms; 2,324 are open to participants now.

This study's planned enrollment of 80 is above the median of 60 across 7,703 interventional studies indexed under Neoplasms.

Browse Neoplasms studies →

Lead sponsor

This is the only study on the registry with Angiex, Inc. as lead sponsor.

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

  • confirmed unresectable, locally advanced, or solid tumors.
  • to or relapsed after all standard therapies known to provide proven clinical benefit, unless the patient is not a candidate for standard treatment, there is no standard treatment, or the patient refuses standard treatment after expressing an understanding of all available therapies with proven clinical benefit
  • Willing to authorize use of existing , unless otherwise discussed with Sponsor
  • Time since the last dose of prior therapy to treat underlying (including other therapy): Systemic cytotoxic chemotherapy: ≥ the duration of the most recent cycle of the previous regimen (with a minimum of 2 weeks for all, except 6 weeks for systemic nitrosourea or systemic mitomycin-C); Biologic therapy (eg, antibodies): ≥ 3 weeks; Small molecule therapies: ≥ 5 × half-life
  • Have an performance status of 0 to 1
  • Have adequate organ function
  • ≥ 50%, as determined on cardiac ECHO or cardiac multiple-gated acquisition (MUGA) scan
  • Highly effective for both male and female patients throughout the study

Exclusion criteria

Exclusion Criteria:

  • Colorectal cancer patients with an unresected primary colorectal tumor and non-small-cell lung cancer with predominant squamous histology (ie, squamous cell carcinoma of the lung) are excluded unless otherwise discussed and approved by Sponsor
  • Clinically unstable central nervous system (CNS) tumors or (stable and/or asymptomatic CNS metastases allowed)
  • Have not recovered to ≤ Grade 1 or baseline from all AEs due to previous therapies (patients with ≤ Grade 2 neuropathy, endocrine-related irAEs, or other AEs may be eligible after discussion with the Sponsor)
  • Has an active vasculitis that has required systemic treatment in the past 2 years prior to starting study treatment
  • Significant (ie, ≥ Grade 2) ocular disturbances
  • Variceal bleeding within 6 months prior to treatment, currently untreated or incompletely treated varices with bleeding, or who otherwise are at a high risk of bleeding
  • Any other concurrent antineoplastic treatment except for allowed local radiation of lesions for palliation (to be considered non-target lesions after treatment) and hormone ablation
  • Uncontrolled or life-threatening symptomatic concomitant disease, including known symptomatic positive with an AIDS defining opportunistic infection within the last year, known symptomatic active or C, or known active tuberculosis
  • Has undergone a major surgery within 3 weeks prior to starting study treatment or has inadequate healing or recovery from complications of surgery prior to starting study treatment
  • Has received prior radiotherapy within 2 weeks prior to starting study treatment
  • Has or had a potentially life-threatening second requiring systemic treatment within the last 3 years, or which would impede evaluation of treatment response
  • cardiovascular disease
  • Patients on a potent inhibitor or CPY3A inducer who cannot be changed to another medication
  • Has an active infection requiring concurrent systemic antibiotic therapy
  • A woman of (WOCBP) who has a positive pregnancy test prior to treatment
  • Is breastfeeding or expecting to conceive or father children within the projected duration of the study
Terms in these criteria, in plain language(15)

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.

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.

Metastases

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

Relapsed and refractory

Relapsed: the illness came back after treatment had worked. Refractory: it did not respond to treatment, or stopped responding while still on it.

Biopsy and archival tissue

A biopsy takes a small piece of tissue to examine. “Archival tissue” is a sample already taken, for example at diagnosis, and kept by the hospital.

Whether a stored sample will do depends on when it was taken, how much there is and what the study needs. Ask whether the study accepts your stored sample or needs a new biopsy.

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.

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.

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.

LVEF (left ventricular ejection fraction)

The share of blood the heart’s main pumping chamber (the left ventricle) pushes out with each beat, measured by an echocardiogram (heart ultrasound) or a MUGA scan. About 50–70% is normal.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Brain metastases

Cancer deposits in the brain from a cancer that started elsewhere in the body (CNS metastases include the spinal cord).

Studies differ: some leave out any brain metastases, some accept ones treated and stable for some weeks. Check what this study allows.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

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.

CYP3A (CYP3A4) inhibitors and inducers

CYP3A is a group of enzymes, mainly CYP3A4, in the liver and gut that break down many medicines. Some medicines, supplements and foods (grapefruit, St John’s wort) slow them down or speed them up, which changes how much of a study drug stays in the body.

Studies list them so they can be avoided or switched; bring a list of everything you take, including supplements.

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
80 participants (estimated)

Study arms

  • Experimental
    Dose Escalation Phase

    AGX-101, initial 90-minute IV infusion, second 60-minute IV infusion and 30 minute subsequent IV infusions on Day 1 of every 3, 6 or 9-week cycle in Dose Escalation Phase. Dose escalation will be carried out in sequential cohorts of escalating doses, with an expansion cohort in advanced angiosarcoma.

    Drug: AGX101

  • Experimental
    Dose Expansion Phase

    AGX-101, initial 90-minute IV infusion, second 60-minute IV infusion and 30 minute subsequent IV infusions on Day 1 of every every 3, 6 or 9-week cycle in Dose Escalation Phase. Dose expansion will be carried out with a selected dose and selected cancer type.

    Drug: AGX101

Interventions

  • DrugAGX101

    Antibody Drug Conjugate

    Also known as: ADC

06

What researchers measure

Primary outcomes

  1. Acceptable maximum tolerated dose for participants

    Maximum tolerated dose (MTD) and the dose-limiting toxicities (DLTs) of AGX101 will be characterized

    Time frame: 21 days following the first dose of AGX101 (Day 1 through Day 21)

  2. Number of participants with adverse events

    Evaluation of the incidence, severity, and duration of adverse events

    Time frame: Screening through end of treatment, approximately 6 months and up to 3 years

Secondary outcomes

  1. Terminal elimination half life (PK)

    Determination of the terminal elimination half-life (t½)

    Time frame: 22 days following the first dose of AGX101 (Day 1 through Day 22)

  2. AUC (PK)

    Determination of the AUC in 1 dosing interval

    Time frame: 22 days following the first dose of AGX101 (Day 1 through Day 22)

  3. Cmax (PK)

    Determination of the Cmax concentration over a dosing interval, systemic clearance, volume of distribution at steady-state (Vss), and accumulation ratio from first dose to steady-state

    Time frame: 22 days following the first dose of AGX101 (Day 1 through Day 22)

  4. Number of Participants with Antidrug Antibodies (ADA) to AGX101

    Incidence and titers of ADA will be measured

    Time frame: Approximately 6 months and up to 3 years

  5. Efficacy as measured by Proportion of Participants with Objective Response Rate (ORR) According to RECIST v1.1 Evaluated by the Investigator

    Determination the objective response rate (ORR)

    Time frame: Approximately 6 months and up to 3 years

  6. Efficacy as measured by Duration of Response (DoR) Assessed by Investigator

    Determination of the duration of response (DoR)

    Time frame: Approximately 6 months and up to 3 years

  7. Efficacy as measured by Disease Control Rate (DCR)

    Determination of the disease control rate (DCR)

    Time frame: Approximately 6 months and up to 3 years

  8. Efficacy as measured by Proportion of Participants with Progression Free Survival (PFS) According to RECIST v1.1 Evaluated by the Investigator

    Determine progression-free survival (PFS)/PFS assessed per immune-related response evaluation criteria (iPFS).

    Time frame: Approximately 6 months and up to 3 years

  9. Efficacy as measured by Duration of Treatment

    Time frame: Approximately 6 months and up to 3 years

  10. Overall Survival

    Time frame: Approximately 6 months and up to 3 years

07

Study locations

7 of 7 sites recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06440005
Lead sponsor
Angiex, Inc.
Responsible party
Sponsor
First posted
Jun 3, 2024
Start date
Jul 22, 2024
Primary completion
Mar 6, 2027 (estimated)
Completion
Sep 6, 2027 (estimated)
Last update
Sep 9, 2026

Study contacts

Glen Weiss, MD
Contact
trials@angiex.com
857-203-7808
Glen Weiss, MD
study director · Medical Lead

Oversight

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

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