ClinicalTrials.gg
RecruitingNCT07073534Updated Jan 22, 2026

Phase I/II Clinical Study of SHR-1501 Combined With Adbelizumab in Patients With Malignant Tumors

A Phase 1/2 interventional study of SHR-1501, Adebrelimab in Patients With Advanced or Metastatic Malignant Tumors, sponsored by Shanghai Hengrui Pharmaceutical Co., Ltd.. Recruiting at 1 site in China. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-01-22.

Sponsored by Shanghai Hengrui Pharmaceutical Co., Ltd. (part of Jiangsu HengRui Medicine Co., Ltd.) · Phase 1/2, Interventional, and Treatment

From the registry’s dates

  • Started Jul 2025; still recruiting 1 year 3 months later.
Phase
Phase 1/2
Study type
Interventional
Enrollment
203
Allocation
Not applicable
Ages
18 Years to 75 Years
Sex
All
01

Study summary

This study is an open, multicenter phase I/II clinical study. The entire study is divided into three stages: dose escalation, dose expansion, and efficacy expansion. Objective: To evaluate the objective response rate (ORR), safety and tolerability of the combination of SHR-1501 and adibelizumab in the treatment of advanced malignant tumors, and to provide the recommended dose (RP2D) for subsequent clinical studies.

02

Conditions studied

  • Patients With Advanced or Metastatic Malignant Tumors

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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 203 is above the median of 60 across 7,703 interventional studies indexed under Neoplasms.

Browse Neoplasms studies →

Lead sponsor

Shanghai Hengrui Pharmaceutical Co., Ltd. is the lead sponsor of 61 studies on the registry; 31 are open to participants now.

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. Voluntarily participate in this clinical study, understand the research procedures and be able to sign the form in person.
  2. Age: 18 to 75 years old (including both ends), gender not limited.
  3. Subjects with locally advanced or solid tumors that have been or cytologically confirmed to be inoperable for radical surgery or radical chemoradiotherapy, whose disease progresses after standard treatment, or who have no standard treatment plan, or are not suitable for standard treatment.
  4. According to the efficacy evaluation criteria for Solid tumors ( 1.1), there is at least one ;
  5. The physical condition score is 0 or 1.
  6. The expected survival time is more than 3 months;

Exclusion criteria

Exclusion Criteria:

  1. Symptomatic or active central nervous system (CNS) tumor ;
  2. Other malignant tumors within five years before the first use of study drugs;
  3. Uncontrolled tumor-related pain judged by the investigator;
  4. Severe cardiovascular and cerebrovascular diseases;
  5. Significant clinical bleeding symptoms within 3 months before the first study drug, and obvious fresh hemoptysis within 1 month before the first study drug;
  6. Uncontrollable pleural effusion and/or ascites judged by the study or pleural effusion and/or ascites requiring intervention within 7 days before the first treatment
  7. History of idiopathic pulmonary fibrosis, organizing pneumonia (such as bronchiolitis obliterans), drug-related pneumonia requiring therapy;,or active pneumonia at screening; or other moderate to severe pulmonary diseases that significantly affect pulmonary function;
  8. Severe infection within 4 weeks before the start of study treatment
  9. History of immunodeficiency
  10. Used corticosteroids (>10 mg/day prednisone or equivalent) or other systemic within 14 days before the first study drug.
  11. Patients with active pulmonary tuberculosis infection within 1 year before enrollment as determined by medical history or imaging examination, or patients with a history of active pulmonary tuberculosis infection more than 1 year ago but without formal treatment
  12. Patients whose adverse events caused by previous treatment have not recovered to ≤ grade 1
  13. Patients whose previous treatment does not meet the following requirements: Patients who have received chemotherapy, biological therapy, targeted therapy, immunotherapy, or other unlisted clinical research drugs and other anti-tumor treatments within 4 weeks before the first use of the study drug
  14. Patients who have experienced CTCAE grade 4 or grade 3 immune-related adverse events lasting for 4 weeks or longer after previous use of , or immune-related adverse events that led to treatment discontinuation, are not eligible for enrollment in this study.
  15. Patients who have received >30 Gy chest radiotherapy within 24 weeks before the first use of the study drug, patients who have received >30 Gy non-chest radiotherapy within 4 weeks before the first use of the drug (subjects who have completed radiotherapy 14 days before the first use of the drug can be enrolled), and patients who have received ≤30 Gy within 14 days before the first use of the drug Gy of palliative radiation;
  16. Subjects who have undergone surgery on important organs (excluding puncture ) within 4 weeks before the first use of the study drug, have had significant trauma, or need to undergo elective surgery during the trial;
  17. Active, known or suspected diseases and history of autoimmune diseases.
  18. Using attenuated within 28 days before the first use of the study drug, or anticipating the need to use attenuated live vaccines during the study treatment;
  19. Pregnant or lactating women or female subjects who plan to become pregnant during the study and within 6 months after the last use of the study drug;
  20. Those who are known to be allergic to any component or of the study drug; or have a history of severe allergic reactions to other monoclonal antibodies/fusion protein drugs;
  21. The investigators judge that the subjects have other factors that may affect the study results or force the termination of this study, such as alcoholism, drug abuse, other serious diseases (including mental illness) requiring combined treatment, serious abnormal laboratory test values, family or social factors, and other situations that may affect the safety of the subjects or the collection of trial data.
Terms in these criteria, in plain language(16)

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.

Metastases

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

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.

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.

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.

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.

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.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

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.

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.

PD-1, PD-L1 and checkpoint inhibitors

PD-1, PD-L1 and CTLA-4 are proteins that act as brakes on the immune system. Checkpoint inhibitors, such as pembrolizumab or nivolumab, block them so the immune system can attack a cancer.

PD-L1 can also be measured in a tumour sample. Some scores count stained tumour cells only (TPS); others also count certain immune cells (CPS). The study names the score and the minimum it uses.

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.

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.

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.

Excipients

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

05

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
203 participants (estimated)

Study arms

  • Experimental
    the combination of SHR-1501 and Adebrelimab

    Drug: SHR-1501, Adebrelimab

Interventions

06

What researchers measure

Primary outcomes

  1. Dose-limiting toxicity

    evaluate the safety in the doses escalation

    Time frame: 21 Days or 28 days

  2. Maximum tolerated dose or Maximum-administered dose

    evaluate the safety in the doses escalation

    Time frame: Approximately 1 years

  3. Recommended Phase 2 dose (RP2D)

    evaluate the safety and curative effect in the doses escalation

    Time frame: Approximately 2years.

  4. Objective response rate(ORR)

    Preliminary evaluation of the effectiveness of the combination of SHR-1501 and Adebrelimab

    Time frame: Approximately 2 years

  5. The incidence and severity of adverse events (AE)/serious adverse events (SAE) (rated based on CTCAE v5.0)

    Preliminary safety of the effectiveness of the combination of SHR-1501 and Adebrelimab

    Time frame: 21 Days,Approximately 2 years

Secondary outcomes

  1. Maximum concentration (Cmax) of SHR-1501

    To evaluate the pharmacokinetic characteristics of the combination of SHR-1501 and Adebrelimab

    Time frame: Approximately 2 years

  2. Time to maximum concentration (Tmax) of SHR-1501

    To evaluate the pharmacokinetic characteristics of the combination of SHR-1501 and Adebrelimab

    Time frame: Approximately 2 years

  3. Areas under the concentration-time curve from time zero to the time of last quantifiable concentration (AUClast) of SHR-1501

    To evaluate the pharmacokinetic characteristics of the combination of SHR-1501 and Adebrelimab

    Time frame: Approximately 2 years

  4. Steady-state valley concentration (Cmin)of SHR-1501

    To evaluate the pharmacokinetic characteristics of Steady-state valley concentration

    Time frame: Approximately 2 years

  5. Accumulation ratio(Rac) of SHR-1501

    To evaluate the pharmacokinetic characteristics of the combination of SHR-1501 and Adebrelimab

    Time frame: Approximately 2 years

  6. Anti-drug antibody of SHR-1501

    To evaluate the pharmacokinetic characteristics of the combination of SHR-1501 and Adebrelimab

    Time frame: Approximately 2 years

  7. Duration of response(DoR)

    Preliminary evaluation of the effectiveness of the combination of SHR-1501 and Adebrelimab

    Time frame: Approximately 2 years

  8. Disease control rate (DCR)

    Preliminary evaluation of the effectiveness of the combination of SHR-1501 and Adebrelimab

    Time frame: Approximately 2 years

  9. Progression free survival (PFS )

    Preliminary evaluation of the combination of SHR-1501 and Adebrelimab

    Time frame: Approximately 2 years

  10. Overall survival(OS)

    Preliminary evaluation of the effectiveness of the combination of SHR-1501 and Adebrelimab

    Time frame: Approximately 2 years

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07073534
Responsible party
Sponsor
First posted
Jul 18, 2025
Start date
Jul 24, 2025
Primary completion
Dec 2027 (estimated)
Completion
Dec 2027 (estimated)
Last update
Jan 22, 2026

Study contacts

Fei Qiu
Contact
fei.qiu@hengrui.com
+0518-81220121

Oversight

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: Efserakefusp alfa · Adebrelimab

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