ClinicalTrials.gg
RecruitingNCT07591090Updated Jul 22, 2026

A Phase II Study of AK146D1 Combined With AK112 in Advanced Breast Cancer

A Phase 2 interventional study of AK146D1 for injection and AK112 Injection in Advanced Breast Cancer, sponsored by Akeso. Recruiting at 1 site in China. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-07-22.

Sponsored by Akeso · Phase 2, Interventional, and Treatment

From the registry’s dates

  • Started Jul 2026; still recruiting 3 months later.
Phase
Phase 2
Study type
Interventional
Enrollment
200
Allocation
Non-randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

This is a Phase II clinical study aimed at evaluating the safety, tolerability, antitumor efficacy, PK and immunogenicity of AK146D1 combined with AK112 in advanced breast cancer.

02

Conditions studied

  • Advanced Breast Cancer

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03

In context

Breast Neoplasms

14,825 studies on the registry are indexed under Breast Neoplasms; 3,319 are open to participants now.

This study's planned enrollment of 200 is above the median of 72 across 10,896 interventional studies indexed under Breast Neoplasms.

Browse Breast Neoplasms studies →

Lead sponsor

Akeso is the lead sponsor of 156 studies on the registry; 66 are open to participants now.

Of its 8 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
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

  1. Be able to understand and voluntarily sign the written form.
  2. Aged of ≥ 18 years and ≤75 years.
  3. PS 0 or 1.
  4. The expected lifespan is ≥3 months.
  5. Patients with confirmed locally advanced, recurrent, or breast cancer who are not eligible for curative surgical resection; and who have histologically or cytologically confirmed -negative disease.
  6. At least one according to v1.1. Patients with only bone lesions or cutaneous lesions are not ineligible for enrollment.
  7. Have sufficient organ function.
  8. Females patients must not be pregnant at screening or have evidence of non-. Agree to use medically accepted methods of .

Exclusion criteria

Exclusion Criteria:

  1. Patients had breast cancer amenable to curative treatment at study enrollment.
  2. Concurrent other histopathological types confirmed by tumor histology or cytology.
  3. Having other active within 3 years.
  4. Currently participating in another interventional clinical study.
  5. Presence of active to the central nervous system. For patients with asymptomatic or stable symptoms after treatment can be included.
  6. Prior treatment with any therapy targeting Trop-2 or Nectin-4, or any chemotherapy agent targeting topoisomerase I.
  7. Receipt of systemic anti-tumor therapy (including chemotherapy, immunotherapy, biological agents, etc.) within 4 weeks prior to the first dose.
  8. Toxicity of previous antineoplastic therapy has not resolved to 6.0 grade 1 or lower.
  9. Patients with cardiovascular or cerebrovascular diseases or risks.
  10. Patients with active diseases requiring systemic treatment within 2 years.
  11. Receipt of systemic anti-infective therapy within 2 weeks prior to the first dose.
  12. Known to be positive for and other infections.
  13. Previous history of severe reactions.
  14. were received within 4 weeks.
  15. Patients with a history of mental illness and incapacitated or limited capacity.
  16. Any disease or condition that, in the opinion of the investigator, would compromise patient safety or interfere with study assessments.
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.

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.

HER2

HER2 is a protein, made from the ERBB2 gene, that drives the growth of some cancers. A study may look for a level of the protein, extra copies of the gene, or a particular change in it.

In breast cancer, protein tests are read as HER2-positive, HER2-low or HER2-negative; other cancers use their own rules. Check which test result the study requires.

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.

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.

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.

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.

CTCAE grade

The US National Cancer Institute’s scale of how severe an adverse event is — any unwanted medical event during a study, such as a symptom, an illness or an abnormal test result, whether or not a treatment caused it. Whether it did is judged separately.

1
Mild.
2
Moderate.
3
Severe.
4
Life-threatening.
5
Death due to the event.

“Side effects of earlier treatment resolved to grade 1 or less” means they have settled to mild or gone.

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.

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.

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.

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.

05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
200 participants (estimated)

Study arms

  • Experimental
    Arm A

    Participants in this group will receive AK146D1 combined with AK112 as i.v. infusion.

    Drug: AK146D1 for injection · Drug: AK112 Injection

  • Experimental
    Arm B

    Participants in this group will receive AK146D1 as i.v. infusion.

    Drug: AK146D1 for injection

Interventions

06

What researchers measure

Primary outcomes

  1. Number of participants with dose limiting toxicities (DLTs)

    DLTs are defined as toxicities that meet pre-defined severity criteria, and assessed as having a suspected relationship to study drug.

    Time frame: During the first 3 weeks of treatment in Safety Run-in Phase.

  2. Number of participants with adverse events (AEs)

    AEs refer to any untoward medical occurrence or deterioration of existing medical events after the participants sign the ICFs, whether or not considered related to the study treatment.

    Time frame: From the time of signing informed consent form through 30 days(for AEs) or 90 days(for SAEs) after the last dose of study drug.

  3. Objective Response Rate (ORR) assessed by investigator per RECIST v1.1

    ORR is the proportion of participants with complete response(CR) or partial response(PR) , assessed based on RECIST v1.1.

    Time frame: Up to approximately 2 years.

Secondary outcomes

  1. Progression Free Survival (PFS) assessed by investigator per RECIST v1.1

    PFS is defined as the time from the start of treatment until the first documentation of disease progression (based on RECIST Version 1.1) or death due to any cause, whichever occurs first.

    Time frame: Up to approximately 2 years.

  2. Disease Control Rate (DCR) assessed per RECIST v1.1

    DCR is defined as the proportion of participants with CR, PR, or SD, assessed based on RECIST v1.1.

    Time frame: Up to approximately 2 years.

  3. Duration of response (DoR) assessed by the investigator per RECIST v1.1

    DoR is defined as the duration from the first documentation of objective response to the first documented disease progression (based on RECIST Version 1.1) or death due to any cause, whichever occurs first.

    Time frame: Up to approximately 2 years.

  4. Time to response (TTR) assessed by the investigator per RECIST v1.1

    TTR is defined as the time to objective response based on RECIST v1.1.

    Time frame: Up to approximately 2 years.

  5. Overall survival (OS)

    OS is defined as the time from the first dose to death from any cause.

    Time frame: Up to approximately 2 years.

  6. Serum PK concentration of AK146D1 and AK112

    Serum PK concentration of AK146D1 and AK112 in participants after administration.

    Time frame: From pre-dose to the end of the last dose, an average of 6 months.

  7. Anti-drug antibodies (ADA)

    The number and percentage of participants with detectable anti-drug antibodies (ADA)

    Time frame: From pre-dose to 30 days post end of treatment.

07

Study locations

1 of 1 sites recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07591090
Lead sponsor
Akeso
Responsible party
Sponsor
First posted
May 15, 2026
Start date
Jul 17, 2026
Primary completion
Sep 1, 2027 (estimated)
Completion
Feb 4, 2029 (estimated)
Last update
Jul 22, 2026

Study contacts

Ting Liu
Contact
clinicaltrials@akesobio.com
+86(0760)8987 3999
Zhimin Shao, Study Principal Investigator
Contact

Oversight

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

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