ClinicalTrials.gg
RecruitingNCT07897071Updated Oct 27, 2026

AXT-1003 Combination With Enzalutamide in Participants With mCRPC

A Phase 1 interventional study of AXT-1003, Enzalutamide and AXT-1003, Enzalutamide in mCRPC, sponsored by Axter Therapeutics (Beijing) Co., Ltd. Recruiting at 4 sites in China. Open to male participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-27.

Sponsored by Axter Therapeutics (Beijing) Co., Ltd · Phase 1, Interventional, and Treatment

From the registry’s dates

  • Started Sep 2026; still recruiting 1 month later.
Updated Oct 27, 2026Newly registeredGo to Updates ↓

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Phase
Phase 1
Study type
Interventional
Enrollment
105
Allocation
Non-randomized
Ages
18 Years and older
Sex
Male
01

Study summary

The purpose of this study is to evaluate the efficacy, and safety of AXT-1003 combined with Enzalutamide in subjects with advanced prostate cancer.

Read the detailed description

This study consists of two phases. The first phase (Phase Ia) is a safety lead-in study of AXT-1003 in combination with Enzalutamide; the second phase (Phase Ib) is a dose expansion study. Phase Ia is a non-randomized, open-label study designed to determine the maximum tolerated dose (MTD) and recommended phase 2 dose (RP2D) of AXT-1003 in combination therapy. Based on data derived from the Phase Ia dose-escalation phase, two dose levels of AXT-1003 will be selected for an expansion study in combination with enzalutamide, to explore the antitumor activity.

02

Conditions studied

  • mCRPC

Keywords

  • AXT-1003
  • EZH2
  • Enzalutamide
  • Phase I
  • Advanced malignancies
03

In context

Lead sponsor

Axter Therapeutics (Beijing) Co., Ltd is the lead sponsor of 3 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
Male
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

  1. Age ≥ 18 years.
  2. performance status 0-1.
  3. Histologically/ confirmed prostate adenocarcinoma; neuroendocrine and small cell carcinoma excluded.
  4. disease with evaluable bone lesions (per PCWG3) or measurable soft tissue lesions (per v1.1).
  5. Ongoing LHRH agonist/antagonist therapy, except prior bilateral orchiectomy.
  6. Serum testosterone at castration level (≤50 ng/dL or 1.7 nmol/L) at screening.
  7. Documented disease progression at screening.
  8. Adequate organ function.
  9. Male subjects with partners must use effective through 3 months after last dose.

Exclusion criteria

Exclusion Criteria:

  1. Received chemotherapy, immunotherapy, definitive radiotherapy, major surgery, targeted therapy or other anti-tumor treatments within 4 weeks prior to first dose.
  2. Received palliative radiotherapy within 2 weeks prior to first dose.
  3. Received traditional Chinese medicine (TCM) therapy with anti-tumor indications within 2 weeks prior to first study treatment.
  4. Participated in any other clinical trial within 28 days prior to first study treatment.
  5. Active or .
  6. History of stroke or other severe cerebrovascular disease within 12 months before enrollment.
  7. Uncontrolled or significantly symptomatic cardiovascular disease.
  8. Known or suspected to AXT-1003, any of its , or any components of enzalutamide soft capsules.
  9. History of other prior , except for curatively treated basal cell carcinoma of skin, squamous cell carcinoma of skin, cervical carcinoma in situ, or other carcinoma in situ with no recurrence for 5 years after treatment.
  10. toxicities from any prior therapy (chemotherapy, immunotherapy, radiotherapy, targeted therapy or other treatment) unresolved to Grade ≤ 1 at enrollment, unless deemed no safety risk by the investigator.
  11. Active infection (requiring intravenous antibiotics or hospitalization), active diseases and inflammatory diseases.
  12. Received (including attenuated live vaccines) within 28 days prior to dosing.
  13. Active or infection.
  14. Known (HIV) infection and active tuberculosis.
Terms in these criteria, in plain language(18)

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.

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.

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.

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.

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.

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.

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.

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.

Excipients

The other ingredients in a medicine besides the active drug, such as fillers, colours or preservatives.

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.

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.

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.

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.

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.

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.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

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.

05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
105 participants (estimated)

Study arms

  • Experimental
    Experimental: Dose Escalation AXT-1003+Enzalutamide

    Dose Escalation AXT-1003+Enzalutamide

    Drug: AXT-1003, Enzalutamide

  • Experimental
    Experimental: Dose Expansion AXT-1003+Enzalutamide

    Experimental: Dose Expansion AXT-1003+Enzalutamide

    Drug: AXT-1003, Enzalutamide

Interventions

  • DrugAXT-1003, Enzalutamide

    Drug pages: AXT-1003 · Enzalutamide

    AXT-1003:Ascending oral doses from 10 mg to 40 mg BID, to determine MTD and RP2D. Enzalutamide: Fixed dose of 160 mg QD orally, administered orally in combination.

  • DrugAXT-1003, Enzalutamide

    Drug pages: AXT-1003 · Enzalutamide

    Select 1 or 2 dose levels from dose escalation part. Enzalutamide: Fixed dose of 160 mg QD orally, administered orally in combination.

06

What researchers measure

Primary outcomes

  1. DLT events

    Incidence of dose-limiting toxicity (DLT) events during the dose escalation phase

    Time frame: Up to 28 days

  2. Incidence and severity of AEs and serious AEs (SAEs)

    AEs refer to any adverse medical events occurring in participants from the initiation of AXT-1003 and Enzalutamide administration during clinical trials. SAEs denote events involving death, life-threatening conditions, significant disability/incapacity, hospitalization or prolonged hospitalization arising after AXT-1003 and Enzalutamide administration in participants. Adverse Events will be graded by National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE version \[6.0\]).

    Time frame: Up to 3 years

Secondary outcomes

  1. rPFS

    Radiographic progression-free survival

    Time frame: 3-5 years

  2. PSA

    Prostate-specific antigen (PSA)-related endpoints:

    Time frame: 3-5 years

  3. Objective response rate (ORR)

    Time frame: 3-5 years

  4. Duration of response (DOR)

    Time frame: 3-5 years

  5. Pharmacokinetic (PK) Parameters : Maximum Observed Plasma Concentration (Cmax)

    Multiple dose PK will be calculated as data permits.

    Time frame: Up to 2 years

  6. PK Parameters: Time to Reach Maximum Observed Plasma Concentration (Tmax)

    Multiple dose PK will be calculated as data permits.

    Time frame: Up to 2 years

  7. PK Parameters: Minimum Observed Plasma Concentration (Cmin)

    Multiple dose PK will be calculated as data permits.

    Time frame: Up to 2 years

  8. PK Parameters: Area Under the Curve (AUC)

    Multiple dose PK will be calculated as data permits.

    Time frame: Up to 2 years

  9. PK Parameters: Apparent Oral Clearance (CL/F)

    Multiple dose PK will be calculated as data permits.

    Time frame: Up to 2 years

Other outcomes

  1. Exploratory Endpoint

    Change from baseline in blood H3K27me3 levels

    Time frame: Up to 2 years

07

Study locations

2 of 4 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Sep 2026 (actual). Primary completion is estimated for Aug 2028, 23 months after the start.

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

Registered
Oct 8, 2026
First posted
Oct 27, 2026
StartActual
Sep 24, 2026
Primary completionEst.
Aug 2028
CompletionEst.
Dec 2029
Last update
Oct 27, 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.
Registered
First appeared on the registry. No changes since
Oct 27, 2026
Show all 1 update
  1. Oct 27, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07897071
Lead sponsor
Axter Therapeutics (Beijing) Co., Ltd
Responsible party
Sponsor
First posted
Oct 27, 2026
Start date
Sep 24, 2026
Primary completion
Aug 2028 (estimated)
Completion
Dec 2029 (estimated)
Last update
Oct 27, 2026

Study contacts

Sara Hua, APM
Contact
sara.hua@axtertx.com
0086+15624980624
Wilson Wang, Head of Clinical Operation
Contact
wilson.wang@axtertx.com
Qian Gao, PhD
study director · Axter Therapeutics (Beijing) Co., Ltd

Oversight

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

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Studies of the drugs tested here: AXT-1003 · Enzalutamide

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