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Not yet recruitingNCT07472647Updated Mar 16, 2026

SYS6090 Combination Therapy in Advanced Lung Cancer

A Phase 1/2 interventional study of SYS6090 + pemetrexed + platinum-based chemotherapy and SYS6090 + paclitaxel + platinum-based chemotherapy in Non-Small Cell Lung Cancer and Small Cell Lung Cancer, sponsored by Shanghai JMT-Bio Inc.. Not yet recruiting. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-03-16.

Sponsored by Shanghai JMT-Bio Inc. (part of CSPC Pharmaceutical Group Limited) · Phase 1/2, Interventional, and Treatment

Phase
Phase 1/2
Study type
Interventional
Enrollment
596
Allocation
Non-randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

This is an open-label, multi-cohort, multicenter Phase Ib/II clinical study designed to evaluate the safety, tolerability, and efficacy of SYS6090 injection in combination with chemotherapy or chemotherapy and bevacizumab or SYS6010 (an EGFR ADC) in participants with advanced lung cancer.

02

Conditions studied

  • Non-Small Cell Lung Cancer
  • Small Cell Lung Cancer
03

In context

Carcinoma, Non-Small-Cell Lung

7,620 studies on the registry are indexed under Carcinoma, Non-Small-Cell Lung; 1,838 are open to participants now.

This study's planned enrollment of 596 is above the median of 62 across 6,019 interventional studies indexed under Carcinoma, Non-Small-Cell Lung.

Browse Carcinoma, Non-Small-Cell Lung studies →

Lead sponsor

Shanghai JMT-Bio Inc. is the lead sponsor of 42 studies on the registry; 29 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 signed written .
  2. Age 18 to 75 years at the time of informed consent, with no restriction on sex.
  3. or cytologically confirmed unresectable locally advanced (stage IIIB/IIIC) or (stage IV) non-small cell lung cancer (NSCLC) according to the AJCC/UICC Cancer Staging System, 8th edition, or extensive-stage small cell lung cancer (SCLC), not amenable to curative surgical resection or definitive chemoradiotherapy.
  4. At least one according to v1.1.
  5. (ECOG) performance status of 0 or 1.
  6. Estimated of at least 3 months.
  7. Has protocol-defined adequate organ and bone marrow function.

Exclusion criteria

Exclusion Criteria:

  1. Use of systemic or other therapies within 14 days prior to the first dose of study treatment, except for physiologic replacement doses or permitted local, inhaled, or prophylactic use.
  2. Unresolved > Grade 1 toxicities related to prior anticancer therapy (except for toxicities judged by the investigator to pose no safety risk).
  3. For Cohorts 5A and 5B: prior permanent discontinuation of EGFR-targeted therapy due to dermatologic toxicity, or presence of dermatologic diseases requiring systemic treatment.
  4. Known active central nervous system or , except for stable and adequately treated without the need for ongoing corticosteroids or antiepileptic therapy.
  5. History of interstitial lung disease or non-infectious pneumonitis requiring corticosteroid treatment; current ILD or non-infectious pneumonitis; or inability to exclude these conditions at screening.
  6. History of severe cardiovascular or cerebrovascular disease.
  7. Active or recurrent disease requiring systemic treatment, except for clinically stable or well-controlled conditions as specified in the protocol.
  8. Prior immunotherapy associated with severe immune-related adverse events (≥ Grade 3) or immune-related myocarditis (≥ Grade 2), excluding stable immune-related endocrine disorders.
  9. bleeding events (≥ Grade 2 according to v6.0) within 4 weeks prior to the first dose of study treatment.
  10. Arterial or venous thromboembolic events within 6 months prior to the first dose of study treatment, unless judged by the investigator to be clinically stable and low risk.
  11. Presence of ascites or pleural effusion requiring drainage within 14 days prior to the first dose.
  12. Known to any component of the study treatment, history of severe hypersensitivity or infusion-related reactions to protein-based therapies, or poorly controlled asthma.
  13. Untreated spinal cord compression.
  14. History of other within 2 years prior to enrollment or concurrent active malignancy, except for cured localized tumors. -
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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

05

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
596 participants (estimated)

Study arms

  • Experimental
    SYS6090 + Pemetrexed + Platinum

    SYS6090 combined with pemetrexed and platinum-based chemotherapy in participants with driver gene-negative non-squamous non-small cell lung cancer (nsqNSCLC).

    Drug: SYS6090 + pemetrexed + platinum-based chemotherapy

  • Experimental
    SYS6090 + Paclitaxel + Platinum

    SYS6090 combined with paclitaxel and platinum-based chemotherapy in participants with driver gene-negative squamous non-small cell lung cancer (sqNSCLC).

    Drug: SYS6090 + paclitaxel + platinum-based chemotherapy

  • Experimental
    SYS6090 + Docetaxel

    SYS6090 combined with docetaxel in participants with driver gene-negative non-small cell lung cancer (NSCLC).

    Drug: SYS6090 + docetaxel

  • Experimental
    SYS6090 + Pemetrexed + Bevacizumab + Platinum

    SYS6090 combined with pemetrexed, bevacizumab, and platinum-based chemotherapy in participants with driver gene-positive non-squamous non-small cell lung cancer (nsqNSCLC).

    Drug: SYS6090 + pemetrexed + bevacizumab + platinum-based chemotherapy

  • Experimental
    SYS6090 + SYS6010 (nsqNSCLC)

    SYS6090 combined with SYS6010 in participants with driver gene-positive non-squamous non-small cell lung cancer (nsqNSCLC).

    Drug: SYS6090 + SYS6010

  • Experimental
    SYS6090 + SYS6010 (NSCLC)

    SYS6090 combined with SYS6010 in participants with driver gene-negative non-small cell lung cancer (NSCLC).

    Drug: SYS6090 + SYS6010

  • Experimental
    SYS6090 + Etoposide + Platinum

    SYS6090 combined with etoposide and platinum-based chemotherapy in participants with small cell lung cancer (SCLC).

    Drug: SYS6090 + etoposide + platinum-based chemotherapy

  • Experimental
    SYS6090 + Chemo/Other Anticancer Therapy

    SYS6090 combined with chemotherapy or other novel anticancer therapies in participants with lung cancer.

    Drug: SYS6090 + chemotherapy or other anticancer therapy

Interventions

06

What researchers measure

Primary outcomes

  1. Dose-Limiting Toxicity (DLT) (Phase Ib)

    To evaluate the safety of SYS6090 in participants.

    Time frame: Approximately 21 days.

  2. Adverse Events (AEs) (Phase Ib)

    To evaluate the safety of SYS6090 combination therapy in participants.

    Time frame: Up to 90 days after the last administration

  3. Objective response rate (ORR) (Phase II)

    ORR is defined as the proportion of participants in whom a complete response (CR) or partial response (PR), per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 is observed as best overall response.

    Time frame: Through out the study (up to 2 years)

Secondary outcomes

  1. Cmax of SYS6090 (and SYS6010 if applicable)

    To evaluate the systemic pharmacokinetics of SYS6090 (and SYS6010 if applicable).

    Time frame: Through out the study (up to 2 years)

  2. AUC0-t of SYS6090 (and SYS6010 if applicable)

    To evaluate the systemic pharmacokinetics of SYS6090 (and SYS6010 if applicable)

    Time frame: Through out the study (up to 2 years)

  3. Clearance (CL) of SYS6090 (and SYS6010 if applicable)

    To evaluate the systemic pharmacokinetics of SYS6090 (and SYS6010 if applicable)

    Time frame: Through out the study (up to 2 years)

  4. Other Efficacy Endpoints Assessed by RECIST v1.1 (DoR, DCR, TTR, PFS, and OS)

    Evaluation of other efficacy endpoints of SYS6090 combination therapy in participants with advanced lung cancer, assessed by the investigator according to RECIST v1.1, including duration of response (DoR), disease control rate (DCR), time to response (TTR), progression-free survival (PFS), and overall survival (OS).

    Time frame: Through out the study (up to 2 years)

  5. Adverse Events (AEs) (Phase II)

    To evaluate the safety of SYS6090 combination therapy in participants

    Time frame: Through out the study (up to 2 years)

  6. Correlation between Biomarker Levels and Preliminary Efficacy

    The Correlation between Baseline PD-L1 Expression and Antitumor Activity

    Time frame: Through out the study (up to 2 years)

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 16, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07472647
Responsible party
Sponsor
First posted
Mar 16, 2026
Start date
Feb 28, 2026 (estimated)
Primary completion
Feb 28, 2029 (estimated)
Completion
Feb 28, 2030 (estimated)
Last update
Mar 16, 2026

Study contacts

Clinical Trials Information Group officer
Contact
ctr-contact@cspc.cn
031169085587

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Studies of the drugs tested here: Anti-PD-1/IL-15 Fusion Protein JMT108 · Pemetrexed · Paclitaxel · Docetaxel · Bevacizumab · Anti-EGFR Antibody-drug Conjugate CPO301 · Etoposide

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