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RecruitingNCT07830199Updated Nov 2, 2026

A Clinical Study of SHR-4595 Injection in Patients With Advanced Solid Tumors to Evaluate Safety, Tolerability and Pharmacokinetics

A Phase 1 interventional study of SHR-4595 for Injection in Solid Tumor, sponsored by Suzhou Suncadia Biopharmaceuticals Co., Ltd.. Recruiting at 2 sites in China. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-11-02.

Sponsored by Suzhou Suncadia Biopharmaceuticals Co., Ltd. (part of Jiangsu HengRui Medicine Co., Ltd.) · Phase 1, Interventional, and Treatment

Updated Nov 2, 2026Now RecruitingSite recruiting status changed+1 moreGo to Updates ↓
Phase
Phase 1
Study type
Interventional
Enrollment
208
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

The study is being conducted to evaluate the safety and tolerability of SHR-4595 for injection in participants with advanced solid tumors, and to determine the dose-limiting toxicity (DLT), maximum tolerated dose (MTD), and recommended dose for Phase II clinical studies (RP2D) of SHR-4595.

02

Conditions studied

  • Solid Tumor
03

In context

Lead sponsor

Suzhou Suncadia Biopharmaceuticals Co., Ltd. is the lead sponsor of 104 studies on the registry; 73 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

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

A subject must satisfy all of the following criteria to be considered for inclusion in the study.

  1. The subjects voluntarily joined the study and signed the ICF.
  2. , as defined by v1.1.
  3. The Eastern Cancer Cooperative Group () performance status of 0 or 1.
  4. ≥ 12 weeks.
  5. Subjects with or histologically confirmed advanced solid tumors who have failed or are intolerant to standard therapy, have no standard therapy, or refuse standard therapy.

Exclusion criteria

Exclusion Criteria:

A subject who meets any of the following criteria will be excluded from study entry.

  1. Symptomatic, untreated or active central nervous system .
  2. Have uncontrolled or severe cardiovascular disease Have clinical symptoms or disease of the heart that are not well controlled.
  3. With any active disease or history of autoimmune disease.
  4. Patients with active or .
  5. Severe infections prior to initiation of study treatment.
Terms in these criteria, in plain language(9)

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.

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.

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.

Life expectancy

The study doctor’s estimate of how long someone is likely to live. Criteria use it so that people can stay in the study long enough for it to answer its question.

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.

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.

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.

05

Study design

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

Study arms

  • Experimental
    SHR-4595 Group

    SHR-4595 for Injection, in different stages with different doses.

    Drug: SHR-4595 for Injection

Interventions

  • DrugSHR-4595 for Injection

    SHR-4595 for injection, in different doses.

06

What researchers measure

Primary outcomes

  1. Adverse events (AEs)

    Safety endpoints.

    Time frame: From Day 1 to 40 days after last dose.

  2. Dose-limiting toxicity (DLT)

    Safety endpoints.

    Time frame: From Day 1 to 12 months.

  3. Maximum Tolerated Dose (MTD)

    Safety endpoints.

    Time frame: From Day 1 to 12 months.

  4. Recommended Phase 2 Dose (RP2D)

    Safety endpoints.

    Time frame: From Day 1 to 12 months.

Secondary outcomes

  1. Progression free survival (PFS)

    Time frame: From Day 1 to 12 months.

  2. Objective response rate (ORR)

    Time frame: From Day 1 to 12 months.

  3. Disease control rate (DCR)

    Time frame: From Day 1 to 12 months.

  4. Duration of response (DOR)

    Time frame: From Day 1 to 12 months.

  5. Overall survival (OS)

    Time frame: From Day 1 to 12 months.

07

Study locations

2 of 2 sites recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Status
Not yet recruiting→Recruiting
changed Nov 2, 2026
Sites
2 sites changed recruiting status (2 now recruiting)
Show 2 sites
  • Cancer Hospital of Dalian University of Technology (Liaoning Cancer Hospital & Institute) · Shenyang, Chinano status→Recruiting
  • Tianjin Cancer Hospital · Tianjin, Chinano status→Recruiting
Nov 2, 2026
Start date
Sep 2026→Oct 20, 2026 (actual)
Nov 2, 2026
Show all 1 update
  1. Nov 2, 2026
    Not yet recruiting→Recruiting
    2 sites changed recruiting status (2 now recruiting)
    Show 2 sites
    • Cancer Hospital of Dalian University of Technology (Liaoning Cancer Hospital & Institute) · Shenyang, Chinano status→Recruiting
    • Tianjin Cancer Hospital · Tianjin, Chinano status→Recruiting
    Start date Sep 2026→Oct 20, 2026 (now actual)
    + 1 other change: verification date

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
NCT07830199
Responsible party
Sponsor
First posted
Sep 21, 2026
Start date
Oct 20, 2026
Primary completion
Dec 2029 (estimated)
Completion
Dec 2030 (estimated)
Last update
Nov 2, 2026

Study contacts

Hongxia Han
Contact
hongxia.han@hengrui.com
+86-0518-82342973
Yuanchao Wang
Contact
yuanchao.wang@hengrui.com
+86-0518-82342973

Oversight

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

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