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RecruitingNCT06888830Updated Jul 8, 2026

A Phase I/II Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Initial Efficacy of JS212 in Subjects With Advanced Malignant Solid Tumour

A Phase 1/2 interventional study of JS212 for Injection in Advanced Malignant Solid Tumours, sponsored by Shanghai Junshi Bioscience Co., Ltd.. Recruiting at 1 site in China. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-07-08.

Sponsored by Shanghai Junshi Bioscience Co., Ltd. · Phase 1/2, Interventional, and Treatment

From the registry’s dates

  • Started Apr 2025; still recruiting 1 year 7 months later.
Phase
Phase 1/2
Study type
Interventional
Enrollment
374
Allocation
Not applicable
Ages
18 Years to 75 Years
Sex
All
01

Study summary

This study is a Phase I/II Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Initial Efficacy of JS212 in Subjects with Advanced Malignant Solid Tumour. Patients will be enrolled in two stages: a dose-escalation stage and a dose expansion stage.

02

Conditions studied

  • Advanced Malignant Solid Tumours
03

In context

Lead sponsor

Shanghai Junshi Bioscience Co., Ltd. is the lead sponsor of 100 studies on the registry; 20 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. Subjects of either sex who are 18 to 75 years of age (inclusive of 18 and 75 years) at the time of signing the consent form;
  2. or cytologically confirmed advanced malignant solid tumors;
  3. (ECOG) performance status score of 0-1;
  4. Expected survival of ≥ 12 weeks;
  5. Subjects have at least 1 according to v1.1 criteria (without measurable lesions are allowed during dose escalation phase);

Exclusion criteria

Exclusion Criteria:

  1. Presence of active central nervous system . If previous radiotherapy or surgery, etc. has been received, and the imaging examination within 4 weeks before the first dose suggests that the is stable without exacerbation or new neurological symptoms, and hormone therapy has been discontinued two weeks before the first dose, screening is allowed; for the presence of meningeal metastasis and brainstem metastasis, regardless of the treatment or not, screening is not allowed;
  2. Presence of clinically symptomatic pleural effusion, ascites, or pericardial effusion that requires repeated management (puncture or drainage, etc.);
  3. Presence of medically uncontrolled hypertension, or with a history of hypertensive crisis or hypertensive encephalopathy;
  4. Presence of a history of (non-infectious) interstitial lung disease (ILD)/non-infectious pneumonia requiring therapy (e.g., idiopathic pulmonary fibrosis, mechanized pneumonia, drug-induced pneumonia, radiation pneumonitis, idiopathic pneumonia, etc.), and current ILD/non-infectious pneumonia;
  5. Presence of lung-specific co-morbidities including, but not limited to, any underlying lung disease (e.g., pulmonary embolism, severe asthma, severe , restrictive lung disease, etc., diagnosed within 3 months prior to the first study dose) and any , connective tissue, or inflammatory disease with pulmonary involvement (e.g., rheumatoid arthritis, Scheugelin's syndrome, sarcoidosis, etc.) and prior total pneumonectomy;
  6. Presence of a history of immunodeficiency, including a positive test for (HIV), or a known history of allogeneic organ transplantation or hematopoietic stem cell transplantation;
  7. the presence of other factors that may cause them to be forced to terminate the study midway, such as serious physical or mental illness or abnormal laboratory tests, which may increase the risk of participation in the study, affect treatment compliance, or interfere with the results of the study, and which, in the judgment of the investigator, make the subject unsuitable for participation in this study;
Terms in these criteria, in plain language(12)

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.

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.

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.

Metastases

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

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.

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.

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.

COPD

Chronic obstructive pulmonary disease: long-term lung disease that makes it hard to breathe out, including emphysema and chronic bronchitis.

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.

Allogeneic and autologous transplant

Stem cell (bone marrow) transplants. Allogeneic uses cells from a donor; autologous uses your own cells, collected earlier and given back.

05

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Sequential assignment
Masking
None (open label)
Enrollment
374 participants (estimated)

Study arms

  • Experimental
    JS212

    If needed, additional descriptive information (including which interventions are administered in each arm) to differentiate each arm from other arms in the clinical trial.

    Drug: JS212 for Injection

Interventions

  • JS212 for Injection is administered on the first day of the first cycle and every 3 weeks thereafter.

06

What researchers measure

Primary outcomes

  1. DLT

    Incidence and severity of DLT events

    Time frame: Up to 1 years

  2. Incidence and severity of Adverse Events

    Abnormal changes in clinical symptoms, vital signs, physical examination, laboratory tests, electrocardiograph and other examinations.

    Time frame: Up to 2 years

  3. MTD

    Maximum tolerated dose

    Time frame: Up to 1 years

  4. RP2D

    Recommended phase II dose

    Time frame: Up to 1 years

  5. ORR

    Objective Response Rate (ORR) as Assessed by Investigator according to RECIST v1.1

    Time frame: Up to 2 years

Secondary outcomes

  1. DOR

    Duration of Objective Response (DOR) as Assessed by Investigator according to RECIST v1.1

    Time frame: Up to 2 years

  2. DCR

    Investigator-assessed Duration of objective Response (DCR) according to RECIST v1.1

    Time frame: Up to 2 years

  3. Progression-Free Survival (PFS)

    Progression-Free Survival (PFS) as Determined by Investigator according to RECIST v1.1

    Time frame: Up to 2 years

  4. Overall Survival (OS)

    Overall Survival (OS)

    Time frame: Up to 2 years

  5. Pharmacokinetic (PK)

    Patient blood concentrations and pharmacokinetic parameters after drug administration

    Time frame: About 6 months after first dosing

  6. Immunogenicity

    Incidence of antidrug antibodies (ADA)

    Time frame: About 6 months after first dosing

Other outcomes

  1. To explore the correlation between potential MARKERS and efficacy

    To explore the correlation between potential MARKERS and efficacy

    Time frame: Up to 2 years

  2. To explore the correlation between serum β-Glucuronidase Concentrations and efficacy

    To explore the correlation between serum β-Glucuronidase Concentrations and efficacy

    Time frame: Up to 2 years

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

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 Jul 8, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06888830
Responsible party
Sponsor
First posted
Mar 21, 2025
Start date
Apr 11, 2025
Primary completion
Dec 31, 2027 (estimated)
Completion
Dec 31, 2028 (estimated)
Last update
Jul 8, 2026

Study contacts

Zhihao Jiang, Master
Contact
zhihao_jiang@junshipharma.com
86-15350403639

Oversight

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

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Discussion

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Studies of the drug tested here: JS212

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