ClinicalTrials.gg
RecruitingNCT07416474Updated Jul 14, 2026

RC148 Plus Platinum-Based Chemotherapy vs Tislelizumab Plus Platinum-Based Chemotherapy for First-Line Squamous Non-Small Cell Lung Cancer (sqNSCLC)

A Phase 3 interventional study of RC148 plus Carboplatin and Paclitaxel and Tislelizumab plus Carboplatin and Paclitaxel in Non-Small Cell Lung Cancer, sponsored by RemeGen Co., Ltd.. Recruiting at 78 sites in China. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-07-14.

Sponsored by RemeGen Co., Ltd. · Phase 3, Interventional, and Treatment

From the registry’s dates

  • Started Apr 2026; still recruiting 7 months later.
Phase
Phase 3
Study type
Interventional
Enrollment
574
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

This study aims to evaluate the efficacy and safety of RC148 combined with platinum-based chemotherapy versus Tislelizumab combined with platinum-based chemotherapy in participants with locally advanced or metastatic Squamous NSCLC who have not received first-line treatment. Participants will: Take RC148 or Tislelizumab combined with platinum-based chemotherapy until the end of the research.

02

Conditions studied

  • Non-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 574 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

RemeGen Co., Ltd. is the lead sponsor of 81 studies on the registry; 40 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 the study and signed the Form (ICF).
  2. Be willing to and able to participate in the trial and comply with the follow up procedures;
  3. Male or female, aged 18-75 years.
  4. Expected survival ≥ 3 months.
  5. PS score 0 or 1.
  6. Histopathologically or confirmed locally advanced or NSCLC not eligible for curative treatment.
  7. No prior systemic anti-tumor treatment for advanced or metastatic squamous NSCLC.
  8. Sufficient cardiac, bone marrow, hepatic, renal, and coagulation function.
  9. Female participants must be , surgically sterilized, or of with a negative blood pregnancy test within 7 days before the first dose. Female participants must agree to use at least one medically approved method during the study treatment and for 6 months after the end of the study treatment, and must not donate oocytes or breastfeed during this period. Male participants must agree to use at least one medically approved contraceptive method during the study treatment and for 6 months after the end of the study treatment, and must not donate sperm during this period.
  10. At least one outside of the brain according to the v1.1 criteria.
  11. A expression test report that meets the requirements must be provided before enrollment.

Exclusion criteria

Exclusion Criteria:

  1. Histopathologically or confirmed non-squamous non-small cell lung cancer.
  2. Squamous NSCLC with known EGFR sensitive mutations and ALK fusions; squamous NSCLC with known driver gene for which approved treatment options exist.
  3. Presence of active .
  4. Imaging at screening shows obvious tumor necrosis and cavitation, and the investigator judges that participation in the study will cause bleeding risk.
  5. Chest radiotherapy > 30Gy within 6 months before randomization; palliative local treatment for non-target lesions within 2 weeks before randomization; non-specific immunomodulatory treatment within 2 weeks before randomization; Chinese herbal medicine or proprietary Chinese medicine treatment with anti-tumor indications within 1 week before randomization.
  6. History of immunotherapy. Note: For adjuvant/ phases or curative radiotherapy/chemoradiotherapy, /PD-1 antibody therapy should be administered only if recurrence or occurs more than 12 months after the completion of the last medication.
  7. Prior systemic anti-tumor treatment other than chemotherapy and PD-1/PD-L1 antibodies.
  8. Systemic treatment with or other drugs within 2 weeks before randomization.
  9. Use of any live or attenuated within 4 weeks before randomization, or planned during the study.
  10. Participation in other clinical trials within 4 weeks before randomization.
  11. Major surgery, interventional therapy, or severe trauma within 4 weeks before randomization, or planned major surgery during the study; core needle or other minor surgery within 7 days before randomization.
  12. Participants with history of severe coagulation dysfunction or current intake of anticoagulant drugs.
  13. Toxic reactions from prior anti-tumor treatment have not recovered to grade 0-1 as defined by version 6.0.
  14. Severe acute or chronic infections.
  15. Active gastrointestinal bleeding, hemoptysis, peptic ulcer, or hemorrhagic events requiring intervention within 4 weeks before randomization; or presence of severe esophagogastric varices or epistaxis.
  16. Severe arterial/venous thrombotic events or cerebrovascular accidents within 6 months before randomization.
  17. Active or heart disease.
  18. Past or current interstitial lung disease, drug-related pneumonia, radiation pneumonitis, severe impairment of lung function, or clinical manifestations or high-risk factors suspected of interstitial lung disease.
  19. History of gastrointestinal perforation and/or fistula, history of gastrointestinal obstruction within 6 months before randomization.
  20. Presence of systemically diseases that are not stably controlled as judged by the investigator.
  21. Active or history of diseases with potential for recurrence.
  22. Past history of other acquired or congenital immunodeficiency diseases or organ transplantation.
  23. Known or delayed-type hypersensitivity to certain components of the study drug or similar drugs.
  24. Presence of symptomatic or intervention-requiring third-space effusions.
  25. Other malignant tumors within 5 years before the start of study drug administration, except for malignant tumors that are expected to be cured after treatment.
  26. Poor compliance and expected inability to cooperate with the completion of trial procedures.
  27. Past or current history of any other diseases, abnormal physical examination findings, or abnormal laboratory examination findings that, in the investigator's judgment, reasonably suggest that the participant has a disease or condition unsuitable for the use of the study drug.
  28. Local or systemic diseases not caused by malignant tumors, or diseases or symptoms secondary to tumors.
  29. For participants who have used PD-1/L1 inhibitors, prior occurrence of grade 3 or above irAE related to immunotherapy, irAE leading to permanent discontinuation of treatment, grade 2 immune-related cardiotoxicity, or irAE of any grade involving the nervous system or eyes; prior occurrence of adverse events requiring treatment with immunosuppressive drugs other than corticosteroids, or recurrence of adverse events during previous immunotherapy requiring systemic use of corticosteroids again.
Terms in these criteria, in plain language(21)

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.

Postmenopausal

Periods have stopped for good: usually no period for 12 months in a row without another medical reason, sometimes confirmed by a blood test (FSH).

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.

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.

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.

Line of therapy

A line of therapy is one course of treatment, which may combine several drugs. First-line is the first course given; second-line follows when that stops working or is not tolerated.

“Two prior lines” means two courses that count separately under the study’s rules — not simply two drugs. Ask the study team if you are unsure how yours are counted.

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.

Adjuvant and neoadjuvant

Neoadjuvant treatment is given before the main treatment (usually surgery), often to shrink a tumour. Adjuvant treatment is given after it, to lower the chance of the cancer coming back.

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.

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.

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.

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.

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.

05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Investigator)
Enrollment
574 participants (estimated)

Study arms

  • Experimental
    RC148 Plus Platinum-Based Chemotherapy

    Drug: RC148 plus Carboplatin and Paclitaxel

  • Active comparator
    Tislelizumab Plus Platinum-Based Chemotherapy

    Drug: Tislelizumab plus Carboplatin and Paclitaxel

Interventions

  • DrugRC148 plus Carboplatin and Paclitaxel

    Drug pages: RC148 · Carboplatin · Paclitaxel

    RC148, Carboplatin, Paclitaxel

    Also known as: RC148 plus Platinum-Based Chemotherapy

  • DrugTislelizumab plus Carboplatin and Paclitaxel

    Drug pages: Tislelizumab · Carboplatin · Paclitaxel

    Tislelizumab, Carboplatin, Paclitaxel

    Also known as: Tislelizumab plus Platinum-Based Chemotherapy

06

What researchers measure

Primary outcomes

  1. Progression Free Survival (PFS)

    PFS is assessed in accordance with RECIST v1.1

    Time frame: 24 months

Secondary outcomes

  1. Overall Survival (OS)

    OS

    Time frame: 24 months

  2. PFS (assessed by the investigator(s))

    PFS assessed by the investigator(s) is assessed in accordance with RECIST v1.1

    Time frame: 24 months

  3. Objective Response Rate (ORR)

    ORR is assessed in accordance with RECIST v1.1

    Time frame: 24 months

  4. Duration of Response (DoR)

    DoR is assessed in accordance with RECIST v1.1

    Time frame: 24 months

  5. Time to Response (TTR)

    TTR is assessed in accordance with RECIST v1.1

    Time frame: 24 months

  6. Treatment-Emergent Adverse Event (TEAE)

    Adverse events during treatment

    Time frame: 46 months

07

Study locations

78 of 78 sites recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 14, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07416474
Lead sponsor
RemeGen Co., Ltd.
Responsible party
Sponsor
First posted
Feb 18, 2026
Start date
Apr 3, 2026
Primary completion
Dec 31, 2027 (estimated)
Completion
Nov 30, 2029 (estimated)
Last update
Jul 14, 2026

Study contacts

Yongfeng Yang
Contact
yongfeng.yang@remegen.com
010-65384976

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: RC148 · Carboplatin · Paclitaxel

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