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RecruitingNCT07462143Updated May 22, 2026

A Phase Ⅱ/Ⅲ Clinical Trial of RC148 Plus Chemotherapy as 1L Therapy for Unresectable or Metastatic Colorectal Cancer

A Phase 2/3 interventional study of RC148 (Dose 1) plus Capecitabine and Oxaliplatin and RC148 (Dose 2) plus Capecitabine and Oxaliplatin in Colorectal (Colon or Rectal) Cancer, sponsored by RemeGen Co., Ltd.. Recruiting at 19 sites in China. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2026-05-22.

Sponsored by RemeGen Co., Ltd. · Phase 2/3, Interventional, and Treatment

From the registry’s dates

  • Started May 2026; still recruiting 5 months later.
Phase
Phase 2/3
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

This is a Phase Ⅱ/Ⅲ study. The purpose of this study is to evaluate the efficacy and safety of RC148 combined with chemotherapy for the first-line treatment of unresectable metastatic colorectal cancer (CRC)

Read the detailed description

Primary objective in Phase II: To preliminarily evaluate the efficacy of RC148 combined with chemotherapy as first - line treatment for unresectable or metastatic CRC.

Primary objective in Phase III: To evaluate the efficacy of RC148 combined with chemotherapy compared with bevacizumab combined with chemotherapy as first - line treatment for unresectable or metastatic CRC.

02

Conditions studied

  • Colorectal (Colon or Rectal) Cancer

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03

In context

Colonic Neoplasms

2,457 studies on the registry are indexed under Colonic Neoplasms; 458 are open to participants now.

This study's planned enrollment of 80 is close to the median of 75 across 1,711 interventional studies indexed under Colonic Neoplasms.

Browse Colonic Neoplasms 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 agree to participate in the study, sign the form, and be able to comply with the study protocol.
  2. Aged 18-75 years old (including 18 years old and 75 years old).
  3. (ECOG) performance status score of 0 or 1.
  4. Expected survival period ≥ 12 weeks.
  5. At least one according to v1.1 criteria.
  6. or cytologically confirmed colorectal adenocarcinoma, judged by the investigator as unsuitable for curative treatment, and no prior systemic anti-tumor treatment in the recurrent or stage.
  7. Subjects must be able to provide tumor tissue samples for biomarker detection.
  8. Adequate bone marrow, liver, kidney, and coagulation function.
  9. Female subjects of 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 have a negative blood pregnancy test within 7 days before study enrollment; male subjects 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.

Exclusion criteria

Exclusion Criteria:

  1. Known to have microsatellite instability-high (MSI-H) or deficient mismatch repair (dMMR).
  2. Imaging shows obvious tumor necrosis or cavitation, and the investigator judges that participation in the study may increase the risk of bleeding.
  3. Subjects with .
  4. Toxicities from prior anti-tumor therapy have not recovered to ≤ grade 1 according to v6.0.
  5. Known or delayed-type allergy to any component of the study drug or similar drugs.
  6. Subjects with nausea and vomiting, chronic gastrointestinal diseases, or other diseases that may interfere the adequate absorption, distribution, metabolism, or excretion of oral drugs.
  7. Subjects with acute, chronic, or symptomatic infections.
  8. Subjects with diagnosed or suspected interstitial lung disease (ILD), drug-related pneumonia, radiation pneumonitis, severe impairment of lung function, or other lung diseases.
  9. Subjects with active inflammatory bowel disease, a history of gastrointestinal perforation and/or fistula, or clinical symptoms of gastrointestinal obstruction.
  10. Subjects with severe arterial/venous thromboembolic events within 6 months before randomization.
  11. Active gastrointestinal bleeding, hemoptysis, peptic ulcer, or hemorrhagic events requiring intervention within 28 days before randomization; or presence of severe esophagogastric varices or epistaxis.
  12. Presence of symptomatic or intervention-requiring third-space effusions.
  13. Subjects with active or previously diagnosed diseases that may recur.
  14. History of other invasive malignant tumors within 5 years before randomization, or presence of any residual evidence of previously diagnosed malignant tumors.
  15. Subjects who are pregnant, lactating, or planning to become pregnant.
Terms in these criteria, in plain language(13)

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.

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.

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.

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.

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.

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.

Relapsed and refractory

Relapsed: the illness came back after treatment had worked. Refractory: it did not respond to treatment, or stopped responding while still on it.

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.

05

Study design

Phase
Phase 2 / Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
80 participants (estimated)

Study arms

  • Experimental
    Experimental Group 1

    Drug: RC148 (Dose1) in combination with CAPEOX

    Drug: RC148 (Dose 1) plus Capecitabine and Oxaliplatin

  • Experimental
    Experimental Group 2

    Drug: RC148 RC148 (Dose 2) in combination with CAPEOX

    Drug: RC148 (Dose 2) plus Capecitabine and Oxaliplatin

Interventions

  • DrugRC148 (Dose 1) plus Capecitabine and Oxaliplatin

    Drug pages: RC148 · Capecitabine · Oxaliplatin

    RC148 (Dose 1) plus Capecitabine and Oxaliplatin

    Also known as: RC148 (Dose 1) plus CAPEOX

  • DrugRC148 (Dose 2) plus Capecitabine and Oxaliplatin

    Drug pages: RC148 · Capecitabine · Oxaliplatin

    RC148 (Dose 2) plus Capecitabine and Oxaliplatin

    Also known as: RC148 (Dose 2) plus CAPEOX

06

What researchers measure

Primary outcomes

  1. Objective Response Rate (ORR)

    Objective Response Rate (ORR) assessed by the investigator according to RECIST v1.1

    Time frame: 24 months

Secondary outcomes

  1. Duration of Response (DoR)

    Duration of Response (DoR) assessed by the investigator according to RECIST v1.1

    Time frame: 24 months

  2. Disease Control Rate (DCR)

    Disease Control Rate (DCR) assessed by the investigator according to RECIST v1.1

    Time frame: 24 months

  3. Time to Response (TTR)

    Time to Response (TTR) assessed by the investigator according to RECIST v1.1

    Time frame: 24 months

  4. Overall Survival (OS)

    OS

    Time frame: 36 months

  5. AEs/SAE

    The incidence and severity of adverse events / serious adverse events

    Time frame: 36 months

07

Study locations

19 of 19 sites recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 22, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07462143
Lead sponsor
RemeGen Co., Ltd.
Responsible party
Sponsor
First posted
Mar 10, 2026
Start date
May 12, 2026
Primary completion
May 12, 2027 (estimated)
Completion
Dec 31, 2030 (estimated)
Last update
May 22, 2026

Study contacts

Hongfang Li
Contact
hongfang.li@remegen.com
010-65018841

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 · Capecitabine · Oxaliplatin

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