Locally Advanced Unresectable or Metastatic Solid TumorsPhase 1NCT05458219
A First-in-human Study of IBI343 in Subjects With Locally Advanced Unresectable or Metastatic Solid Tumors
A Phase 1 study testing IBI343, FOLFIRINOX/mFOLFIRINOX and mFOLFOX in people with Locally Advanced Unresectable or Metastatic Solid Tumors, run by Innovent Biologics (Suzhou) Co. Ltd. at 39 sites in 3 countries.
Trial summary
This is a Phase Ia/Ib, multicenter, open-label, first-in-human study to evaluate the safety, tolerability, PK, and efficacy of IBI343 in participants with locally advanced unresectable or metastatic solid tumors. It is planned to be carried out in different countries or regions such as China, Australia and US. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Locally Advanced Unresectable or Metastatic Solid Tumors
- What is being tested?
- IBI343, FOLFIRINOX/mFOLFIRINOX and mFOLFOX
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 470 participants
- Where
- 39 sitesin 3 countries
- Study dates
- 26 Oct 2022to 31 Dec 2027
- Phase
- Phase 1
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Inclusion criteria to be met for both Phase Ia and Phase Ib:
- Has signed written Informed Consent Form (ICF), willing and able to comply with protocol-specified visits and related procedures.
- Phase Ia dose escalation phase, Phase Ia part 3 1L G/GEJ AC and 1L PDAC cohorts Safety Lead-in stage: Has at least 1 evaluable lesion according to RECIST v1.1; Phase Ia dose expansion and dose optimization phase, Phase Ia part 3 1L G/GEJ AC and 1L PDAC cohorts Dose optimization stage, Phase Ib: Has at least 1 measurable lesion according to Response Evaluation Criteria in Solid Tumors RECIST v1.1.
- Age ≥ 18 years, of either sex.
- Has an Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1.
- Has an expected survival ≥ 12 weeks.
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- Has adequate bone marrow and organ function. Defined as:
- Hematology: ANC ≥ 1.5 × 109/L; Platelet count ≥ 100 × 109/L; Hemoglobin ≥ 9.0 g/dL, participants must not have received transfusion of blood products (including red blood cell suspension, apheresis platelets, cryoprecipitate, etc.), erythropoietin (EPO), G-colony stimulating factor (G-CSF) or granulocyte-macrophage colony stimulating factor (GM-CSF) within 7 days prior to blood sample collection;
- Hepatic function: TBIL ≤ 1.5 × ULN (TBIL ≤ 3 × ULN is allowed for participants with Gilbert's syndrome); ALT and AST ≤ 2.5 × ULN for participants without liver metastasis and ≤ 5 × ULN for participants with liver metastasis; Albumin ≥ 28 g/L;
- Renal function: estimated creatinine clearance ≥ 30mL/min (using Appendix 5. Calculation of Estimated Creatinine Clearance and Body Surface ).
- Coagulation function: international normalized ratio (INR) ≤ 1.5 and activated partial thromboplastin time (APTT) ≤ 1.5 × ULN (participants receiving anticoagulant therapy with coagulation function within the above range are allowed).
- Female participants of childbearing potential or male participants whose partners are female of childbearing potential are required to use effective contraceptive measures throughout the treatment period and for 6 months after the final treatment period.
- Participants with histopathologically confirmed unresectable locally advanced or metastatic malignant solid tumors that have failed or were intolerant to standard therapy or for whom no standard therapy is available.
- Inclusion Criteria for Phase Ia Dose Expansion, Dose Optimization :
- Participants with histopathologically confirmed unresectable locally advanced or metastatic G/GEJ AC, PDAC, BTC, or other solid tumors who have failed or were intolerant to standard therapy or for which no standard therapy is available.
- * CLDN18.2-positive confirmed by pathological examination (in dose expansion phase, G/GEJ AC and PDAC preferentially enrolled * moderate to high expression of CLDN18. 2; in dose optimization phase , G/GEJ AC preferentially enrolled high expression of CLDN18.2 and PDAC preferentially enrolled ***moderate to high expression of CLDN18.2). For participants with previous anti-CLDN18.2 treatment (including but not limited to monoclonal antibodies, ADCs, CAR-T, etc.), tumor samples should be obtained post anti-CLDN18.2 therapy for CLDN18.2 expression evaluation.
- Participants with histopathologically confirmed unresectable locally advanced or metastatic G/GEJ AC who has not received previous systemic therapy. (For Safety Lead-in stage, participants who has received previous systemic therapy are permitted.) A prior (neo)adjuvant systemic therapy completed within 6 months prior to disease relapse or progression will be considered as having received previous systemic therapy.
- Confirmed Her 2-negative (defined as IHC 0 or 1+, or IHC 2+ and negative by in situ hybridization) disease.
- Confirmed combined positive score (CPS) <5 as determined by local IHC testing.
- Participants must not have previously received topoisomerase inhibitor-based antibody-drug conjugate(s), unless given peri-operatively without evidence of resistance.
- Participants must not have previously received anti-CLDN18.2 therapy.
- *CLDN18.2-positive confirmed by pathological examination by central laboratory (For Dose optimization stage, G/GEJ AC enrolled participants with Claudin18.2 immunohistochemical membrane staining intensity 2+/3+ in ≥50% of tumor cells).
- Participants with histopathologically confirmed metastatic PDAC who has not received previous systemic therapy in the metastatic setting. (For Safety Lead-in stage, participants who has received previous systemic therapy are permitted.) A prior (neo)adjuvant systemic therapy completed within 12 months prior to disease relapse or progression will be considered as having received previous systemic therapy.
- Participants must not have previously received anti-CLDN18.2 therapy.
- Participants must not have previously received topoisomerase inhibitor-based antibody-drug conjugate(s), unless given peri-operatively without evidence of resistance.
- *CLDN18.2-positive confirmed by pathological examination by central laboratory (For Dose optimization stage, PDAC enrolled # specified expression of CLDN 18.2)
- Histopathologically confirmed unresectable locally advanced or metastatic G/GEJ AC.
- Have received at least 2 lines of systemic therapy [anti-PD-(L)1 + platinum, fluoropyrimidines, paclitaxel/docetaxel, or irinotecan; participants with HER2 overexpression (defined as 3 + or 2 + by immunohistochemistry and ISH +) must have received anti-HER2 therapy, and participants who have not received prior anti-PD-(L)1 or anti-HER2 therapy must have had a contraindication or reasonable reason for no benefit] and have had disease progression.
- High expression of **CLDN18. 2 was confirmed by pathological examination.
- Histopathologically confirmed unresectable locally advanced or metastatic G/GEJ AC.
- Disease progression after first-line standard therapy (HER2-overexpressing participants must have received prior anti-HER2 therapy unless contraindicated or justified non-benefit).
- Confirmed * CLDN18.2-positive by histopathological examination.
- Histopathologically confirmed unresectable locally advanced or metastatic PDAC.
- Disease progression after at least one prior systemic therapy.
- Histopathologically confirmed unresectable locally advanced or metastatic BTC.
- Disease progression after at least one prior systemic therapy.
- Confirmed * CLDN18.2-positive by histopathological examination.
- Notes:
- CLDN18.2-positive: defined as ≥ 1% of tumor cells with membranous staining of any intensity in tumor tissue by immunohistochemistry, when tested previously, at the study site, or at the central laboratory.
- High expression of CLDN18. 2: Claudin18.2 immunohistochemical membrane staining intensity ≥ 2 + in ≥ 75% of tumor cells.
- Moderate to high expression of CLDN18.2: Claudin18.2 immunohistochemical membrane staining intensity ≥ 2 + in ≥ 40% of tumor cells.
- Specified expression of CLDN18.2: Claudin18.2 immunohistochemical membrane staining intensity 1+/2+/3+ in ≥50% of tumor cells.
Who cannot join
- Is participating in another interventional clinical study other than an observational (non-interventional) clinical study or is in the survival follow-up phase of an interventional study.
- Has received the last dose of antineoplastic therapy within 4 weeks or 5 half-lives of an antineoplastic therapy (whichever is shorter) prior to the first dose of study drug.
- Plans to receive other anti-tumor therapy during treatment with the study drug [palliative radiotherapy for symptomatic relief (e.g., pain) that does not affect response assessment is allowed].
- Has received a strong cytochrome P450 3A4 (CYP3A4) inhibitor within 2 weeks or 5 half-lives (whichever is longer) prior to the first dose of study drug.
- Toxicities due to prior therapy that have not recovered to Grade 0 or 1 per NCI CTCAE v5.0 prior to the first dose of study drug (excluding alopecia, asthenia, hyperpigmentation, and other conditions with no safety risk per the judgment of the investigator).
- Has undergone major surgical procedure (craniotomy, thoracotomy, laparotomy or others per the investigator, excluding needle biopsy) or has unhealed wounds, ulcers, or bone fracture within 4 weeks prior to the first dose of study drug; Or plans to undergo major surgery during the study period; Note: Local surgical treatment of isolated lesions for palliative purposes is acceptable.
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- Has gastric pyloric obstruction and/or persistent recurrent vomiting (≥ 3 episodes in 24 hours).
- Has a history of gastrointestinal perforation and/or fistula within 6 months that has not resolved surgically prior to the first dose of study drug.
- Has symptomatic central nervous system metastases. Participants with asymptomatic brain metastases (i.e., no neurological symptoms, no need for glucocorticoid treatment, all brain metastasis ≤ 1. 5 cm) or stable symptoms after treatment of brain metastases must meet all of the following criteria to participate in the study: no metastasis in the midbrain, pons, cerebellum, meninges, medulla oblongata or spinal cord; Stable clinical status for at least 4 weeks with definitive clinical evidence of no new or enlarging brain metastasis and discontinuation of corticosteroids and anticonvulsants for at least 2 weeks prior to the first dose of study drug. Note: lesions of the central nervous system will not be considered as a target lesion
- Has a history of pneumonitis requiring corticosteroids therapy, or a history of interstitial lung disease, non-infectious pneumonitis, severely impaired lung function or uncontrolled lung disease, such as pulmonary fibrosis, severe radiation pneumonitis, acute lung injury, or suspected of having the above diseases during the screening period.
- Has uncontrolled medical conditions, such as:
- Active or clinically uncontrolled serious infection requiring treatment with systemic anti-infectives (antibiotics, antivirals, or antifungals) within 1 week prior to the first dose of study drug, including but not limited to the infection of respiratory tract, urinary system, biliary tract infection, etc.
- Participants infected with human immunodeficiency virus (HIV) (HIV 1/2 antibody positive).
- Acute or chronic active hepatitis B (defined as hepatitis B surface antigen (HBsAg) and/or hepatitis B core antibody positive (HBcAb) with hepatitis B virus DNA copies ≥ 104 copies/mL or ≥ 2000 IU/mL or above the lower limit of detection) or acute or chronic active hepatitis C [hepatitis C virus antibody (HCVAb) positive with HCV RNA > 103 copies/mL]. Participants whose test results are below the above criteria after receiving antiviral therapy with nucleotides, or participants with positive serology but negative HCV-RNA test result are eligible.
- Has active pulmonary tuberculosis, is being treated with anti-tuberculosis therapy or having received anti-tuberculosis therapy within 1 year prior to the first dose of study drug.
- Has active syphilis or latent syphilis requiring treatment.
- Has symptomatic congestive heart failure (New York Heart Association classification NYHA class II-IV), symptomatic or uncontrolled arrhythmia, QTc interval > 480 ms, or personal or family history of congenital long/short QT syndrome.
- For part 3 1L G/GEJ AC and 1L PDAC cohort, the QTc should be calculated based on the average of triplicate screening ECG (using Appendix 4 Calculation Formula of QTcF)
- Uncontrolled hypertension (systolic blood pressure ≥ 160 mmHg or diastolic blood pressure ≥ 100 mmHg) by standard treatment.
- Has one or more arterial thromboembolic event, including myocardial infarction, unstable angina, cerebrovascular accident, transient ischemic attack, etc., within 6 months prior to the first dose of study drug.
- Has received stent implantation in tracheal or digestive tract.
- Has symptomatic pleural, ascites, or pericardial effusion requiring intervention (e.g., drainage, peritoneal shunt, or cell-free and concentrated ascites reinfusion therapy [CART]). Asymptomatic participants with a small amount of pleural effusion, ascites or pericardial effusion on imaging are allowed. (Drainage and CART are not allowed within 2 weeks prior to screening assessment).
- Has esophageal or gastric varices that require immediate intervention (e.g., ligature or sclerotherapy) or are considered to be at high risk for bleeding in the opinion of the investigator or consulting gastroenterologist or hepatologist. Participants with evidence of portal hypertension (including splenomegaly on imaging) or a history of prior variceal bleeding must undergo endoscopic evaluation within 3 months prior to the first dose of study drug.
- Has one or more life-threatening bleeding event or Grade 3 or 4 gastrointestinal/variceal bleeding requiring blood transfusion, endoscopic or surgical treatment within 3 months prior to the first dose of study drug
- Has a history of deep vein thrombosis, pulmonary embolism, or any other serious venous thromboembolism within 3 months prior to the first dose of study drug (implantable venous access port or catheter-derived thrombosis, or superficial vein thrombosis is not considered "serious" venous thromboembolism).
- Has hepatic encephalopathy, hepatorenal syndrome, or Child-Pugh B or more severe cirrhosis.
- Has complete or incomplete intestinal or bowel obstruction at the time of screening or a history of complete or incomplete intestinal or bowel obstruction within 3 months prior to first dose, or is at risk of intestinal perforation (including but not limited to acute diverticulitis, history of intra-abdominal abscess), or a history of any of the following disease: inflammatory bowel disease or extensive bowel resection (partial colectomy or extensive small bowel resection with concurrent chronic diarrhea), Crohn's disease, ulcerative colitis, and chronic diarrhea.
- Has other acute or chronic disease or laboratory abnormality that may result in increased risk associated with study participation or study drug administration, or interfere with the interpretation of study results, and is considered unfit for this study per the Investigator's judgement.
- Has a neurological or psychiatric illness or a social situation that affects compliance with study requirements, significantly increases the risk of AE, or affects the participant's ability to provide written ICF.
- Has a history of other primary malignancies, with the following exceptions:
- Curatively treated malignancy with no known active disease for ≥ 2 years prior to study enrollment and is at minimal risk of recurrence;
- Adequately treated non-melanoma skin cancer or lentigo maligna without evidence of disease recurrence;
- Adequately treated carcinoma in situ with no evidence of disease recurrence.
- Has a known history of immunodeficiency.
- Has a history of allogeneic organ transplantation and history of allogeneic hematopoietic stem cell transplantation.
- Has a history of severe allergic reaction to other monoclonal antibodies and/or hypersensitivity to any of the formulation components of IBI343 or mFOLFOX or Irinotecan or liposomal Irinotecan (For phase 1a part 3 1L G/GEJ AC and 1L PDAC cohort).
- Female participants who are pregnant or lactating.
- Has other conditions considered not eligible to participate in this study per the Investigator's judgement.
- Has known dihydropyrimidine dehydrogenase deficiency (DPD). (NOTE: Screening for DPD deficiency should be conducted per local requirements.)
- Has known peripheral sensory neuropathy > grade 1 unless the absence of deep tendon reflexes is the sole neurological abnormality.
Trial locations and contacts
39 sites in 3 countries. Contact the study team or a site near you to ask about taking part.
39 sites in 3 countries
China32 sites, 32 recruiting
- Recruiting
Beijing Cancer Hospital
Beijing, Beijing Municipality
Lin Shen
- Recruiting
Tumor Hospital, Chinese Academy of Medical Sciences
Beijing, Beijing Municipality
Aiping Zhou
- Recruiting
Hunan Cancer Hospital
Changsha, Hunan
Zhenyang Liu
YongChang Zhang
- Recruiting
West China Hospital of Sichuan University
Chengdu, Sichuan
Xuelei Ma
- Recruiting
Fujian Cancer Hospital
Fuzhou, Fujian
Jianwei Yang
- Recruiting
Sun Yat-sen Memorial Hospital Sun Yat-Sen university
Guangzhou, Guangzhou
Zhihua Li
- Recruiting
The First Affiliated Hospital of Sun Yat-sen University
Guangzhou, Guangzhou
Xiaoyu Yin
- Recruiting
The First Affiliated Hospital, Zhejiang University School of Medicine
Hangzhou, Zhejiang
Jian Ruan
- Recruiting
Zhejiang Cancer Hospital
Hangzhou, Zhejiang
Jieer Ying
- Recruiting
Zhejiang Provincial People's Hospital
Hangzhou, Zhejiang
Yiping Mou
- Recruiting
Anhui Cancer Hospital
Hefei, Anhui
Suyi Li
- Recruiting
Anhui Provincial Hospital
Hefei, Anhui
Yueyin Pan
- Recruiting
Jinan Central Hospital
Jinan, Shandong
Meili Sun
- Recruiting
Shandong Cancer Hospital
Jinan, Shandong
Yuping Sun
Jinbo Yue
- Recruiting
Jining First People's Hospital
Jining, Shandong
Jie Li
- Recruiting
Jiangxi Cancer Hospital
Nanchang, Jiangxi
Rongfeng Song
- Recruiting
The Second Affiliated Hospital of Nanchang University
Nanchang, Jiangxi
Jianbing Wu
- Recruiting
Nanjing Drum Tower Hospital
Nanjing, Jiangsu
Juan Du
- Recruiting
Ningbo Medical Center Li Huili Hospital
Ningbo, Zhejiang
Yongfei Hua
Weiming Yu
- Recruiting
The Affiliated Hospital of Qingdao University
Qingdao, Shandong
Zimin Liu
- Recruiting
Fudan University Shanghai Cancer Center
Shanghai, Shanghai Municipality
Xianjun Yu
- Recruiting
Renji Hospital, Shanghai Jiaotong University School of Medicine
Shanghai, Shanghai Municipality
Xiuying Xiao
- Recruiting
Ruijin Hospital, Shanghai Jiaotong University School of Medicine
Shanghai, Shanghai Municipality
Jun Zhang
- Recruiting
The First Hospital of China Medical University
Shenyang, Liaoning
Xiujuan Qu
- Recruiting
Tianjin Cancer Hospital
Tianjin, Tianjin Municipality
Ting Deng
- Recruiting
Hubei Cancer Hospital
Wuhan, Hubei
Xinjun Liang
- Recruiting
Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technolog
Wuhan, Hubei
Xianglin Yuan
- Recruiting
The First Affiliated Hospital of Wannan Medical College
Wuhu, Anhui
Lili Sheng
- Recruiting
The First Affiliated Hospital of Xi'an Jiaotong University
Xi'an, Shaanxi
Enxiao Li
- Recruiting
Ningxia Medical University General Hospital
Yinchuan, Ningxia
Ping Chen
- Recruiting
Henan Provincial People's Hospital
Zhengzhou, Henan
Chuangxin Lu
- Recruiting
The First Affiliated Hospital of Zhengzhou University
Zhengzhou, Henan
Yanru Qin
Australia4 sites, 3 recruiting
- Active, not recruiting
Pindara Private Hospital
Benowa, Queensland, 4217
- Recruiting
Sunshine Coast University Private Hospital
Birtinya, Queensland, 4575
morrismi2@ramsayhealth.com.au
Michelle Morris, Dr
- Recruiting
St Vincent's Hospital Sydney
Darlinghurst, New South Wales, 2010
jia.liu@svha.org.au
Jia(Jenny) Liu, Dr
- Recruiting
Cancer Care Wollongong
Wollongong, New South Wales, 2500
Gary Tincknell, Dr
United States3 sites, 3 recruiting
- Recruiting
Next Oncology-Austin
Austin, Texas, 78758
Sheena Sahota
- Recruiting
Next Oncology-Dallas
Irving, Texas, 75039
Shiraj Sen
- Recruiting
Next Oncology-San Antonio
San Antonio, Texas, 78229
Ildefonso I Rodriguez Rivera
About this study
Official title: A Phase 1a/b, Multicenter, Open-label, First-in-human Study of IBI343 in Subjects With Locally Advanced Unresectable or Metastatic Solid Tumors
This is a Phase Ia/Ib, multicenter, open-label, first-in-human study to evaluate the safety, tolerability, PK, and efficacy of IBI343 in participants with locally advanced unresectable or metastatic solid tumors. It is planned to be carried out in different countries or regions such as China, Australia and US.
There are three parts in phase Ia. Part 1 includes dose escalation and expansion phase and part 2 is designed for dose optimization for IBI343 monotherapy.
Part 3 1L G/GEJ AC and 1L PDAC cohorts will include an initial safety lead-in stage to confirm the tolerability of IBI343 in combination with chemotherapy in 1L PDAC and G/GEJ AC, followed by a randomized dose-optimization stage designed to further characterize safety, pharmacokinetics, and preliminary efficacy to inform selection of the recommended Phase 3 dose.
- Being tested
- IBI343, FOLFIRINOX/mFOLFIRINOX, mFOLFOX
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
IBI343Drug
IBI343 will be administered intravenously (IV) on Day 1 of every 21-day cycle.
FOLFIRINOX/mFOLFIRINOXDrug
FOLFIRINOX/mFOLFIRINOX will be administered IV Q2W on Days 1-3 every 2 weeks (14 days).
mFOLFOXDrug
mFOLFOX will be administered IV Q2W on Days 1-3 every 2 weeks (14 days) in each cycle after IBI343
IBI343Drug
IBI343 will be administered IV Q2W on Day1 (14 days).
| Study group | Role | What they receive |
|---|---|---|
| 3 arms | Experimental | Phase 1a Part 3: For monotherapy: 6 mg/kg Q3W was confirmed as the optimal dosing regimen for balancing clinical benefits and potential risks.
In 1L G/GEJ AC and 1L PDAC cohort of the Phase Ia (Part 3) study, IBI343 combination therapy is proposed to be administered at doses of 4 mg/kg (Dose level 1) Q2W or 5 mg/kg (Dose level 2) Q2W in participants with G/GEJ AC and PDAC for the randomized study. Receives: Drug: FOLFIRINOX/mFOLFIRINOX; Drug: mFOLFOX; Drug: IBI343 |
| Single arm | Experimental | Phase 1a Part 1 Dose Escalation: IBI343 will be administered intravenously (IV) at different dose levels following traditional 3+3 dose escalation design for following levels.
Phase 1a Part 1 Dose Expansion: IBI343 will be administered at dose levels which is equal or lower than MTD. Each dose level contains no more than 30 subjects (including subjects in dose escalation) Phase 1a Part 2 Dose Optimization: IBI343 will be administered in parallel cohorts (randomized 1:1 ratio) to determine the optimal dose for the PDAC indication across China, Australia and the US (n=40). Dose levels 4.5mg/kg and 6mg/kg will be studied.
Phase 1b Dose Extension: IBI343 will be administered at RP2D. Receives: Drug: IBI343 |
What is being measured
The primary outcome is the main question the study is designed to answer.
Adverse events(AEs), treatment emergent adverse event (TEAEs)，serious adverse events (SAEs)
Adverse events will be assessed by investigator(s) according to NCI-CTCAE v5.0.
Measured: Up to 90 days after the last administration
Dose-limiting Toxicity (DLT)
DLTs are assessed during the DLT observation period to determine maximum tolerated dose (MTD) and/or recommended phase 2 dose (RP2D).
Measured: 21 days after the first dose of IBI343
To determine RP2D of IBI343.
To determine RP2D of IBI343.
Measured: Up to 2 years
ORR assessed by the investigator based on RECIST version 1.1.
ORR assessed by the investigator based on RECIST version 1.1.ORR is defined as the proportion of participants with a complete response (CR) or partial response (PR)
Measured: Up to 2 years
Number of subjects with clinically significant changes in physical examination results
A complete physical examination will include: general appearance, respiratory, cardiovascular, abdomen, skin, head and neck (including ears, eyes, nose, and pharynx), lymph nodes, thyroid, musculoskeletal (including spine and extremities), genital/anal, and neurological assessments, if indicated. Clinically significant abnormal findings at screening will be recorded as medical history or AE based on the investigator's analysis and judgment.
Measured: Up to 2 years
Number of participants with abnormal vital signs
Collection of vital signs will include temperature in ℃, measurement tool is physiological parameter
Measured: Through study completion, up to 2 years
Objective response rate (ORR)
Through study completion, up to 2 years
Measured: ORR is defined as the proportion of participants with a completeresponse (CR) or partial response (PR)
Number of participants with abnormal laboratory tests results
Blood routine：RBC, HGB, HCT, WBC, PLT, LYM, ANC
Measured: Through study completion, up to 2 years
Number of participants with abnormal vital signs
Collection of vital signs will include pulse in beats per minute. measurement tool is physiological parameter
Measured: Through study completion, up to 2 years
Number of participants with abnormal vital signs
Collection of vital signs will include respiratory rate in times/min. measurement tool is physiological parameter
Measured: Through study completion, up to 2 years
Number of participants with abnormal vital signs
Collection of vital signs will include blood pressure in kPa. measurement tool is physiological parameter
Measured: Through study completion, up to 2 years
Number of participants with abnormal laboratory tests results
Blood biochemistry: TBIL, DBIL, ALT, AST, γ-GGT, ALP, ALB, TP, LDH, Urea or BUN, Cr, Na, K, Cl, Mg, Ca, P, Amylase, Lipase and FBG
Measured: Through study completion, up to 2 years
Number of participants with abnormal laboratory tests results
Urinalysis: PH, Specific Gravity, UWBC, UPRO, URBC, UGLU, UBLD
Measured: Through study completion, up to 2 years
Number of participants with abnormal laboratory tests results
Coagulation function: APTT, PT, INR, Fbg, D-dimer
Measured: Through study completion, up to 2 years
Number of participants with abnormal laboratory tests results
Viral serology test: HBsAg, HBsAb, HBcAb, HBeAg, HBeAb, HBV DNA, HCV antibody, HCV RNA, HIV antibody, Treponema pallidum-specific antibody
Measured: Through study completion, up to 2 years
Number of participants with abnormal laboratory tests results
Myocardial injury markers: CK, CK-MB, Troponin I or T, BNP or NT-proBNP
Measured: Through study completion, up to 2 years
Number of participants with abnormal laboratory tests results
Fecal analysis: occult blood (OB)
Measured: Through study completion, up to 2 years
Secondary outcomes (16)
maximum concentration (Cmax)
PK parameters maximum concentration (Cmax) of IBI343, total antibody, can will be determined.
Measured: Up to 2 years
area under the curve (AUC)
PK parameters area under the curve (AUC) of IBI343, total antibody, exatecan will be determined.
Measured: Up to 2 years
clearance rate (CL)
PK parameters clearance rate of IBI343, total antibody, exatecan will be determined .
Measured: Up to 2 years
half-life (t1/2)
PK parameters half-life (t1/2) of IBI343, total antibody, exatecan will be determined .
Measured: Up to 2 years
Anti-drug antibody(ADA) of IBI343
The incidence and characterization of ADA of IBI343 will be determined
Measured: Up to 2 years
Objective response rate (ORR)
ORR is defined as the proportion of participants with a complete response (CR) or partial response (PR).
Measured: Through study completion, up to 2 years
time to response (TTR)
TTR is defined as the time from the date of first dose of study drug to the date of first documented tumor response (CR/PR).
Measured: Through study completion, up to 2 years
duration of response (DoR)
DoR is defined as the time from the date of first documented tumor response (CR/PR) until PD/death.
Measured: Through study completion, up to 2 years
disease control rate (DCR)
DCR is defined as the proportion of participants with a complete response (CR) or partial response (PR) or stable disease(SD)
Measured: Through study completion, up to 2 years
progression-free survival (PFS)
PFS is defined as the time from the date of first dose of study drug to the date of the first documented progression or death due to any cause, whichever occurs first.
Measured: Through study completion, up to 2 years
Overall survival (OS)
OS is defined as the time from the date of first dose of study drug until the date of death from any cause.
Measured: Through study completion, up to 2 years
apparent volume of distribution (V)
PK parameters apparent volume of distribution(V) of IBI343, total antibody, exatecan will be determined when appropriate.
Measured: Up to 2 years
Tmax
PK parameters time to maximum concentration of IBI343, total antibody, exatecan will be determined when appropriate.
Measured: Up to 2 years
assess the immunogenicity of IBI343.
The incidence of ADA.
Measured: Up to 2 years
To evaluate the correlation between CLDN18.2 expression level in tumor tissue and anti-tumor activities of IBI343 combination therapy.
Baseline CLDN18.2 expression level and relationship with efficacy.
Measured: Up to 2 years
To evaluate the correlation between CLDN18.2, PD-L1, HER2 expression level in tumor tissue in 1L G/GEJ AC cohort.
Baseline CLDN18.2, PD-L1, HER2 expression level and their correlation in 1L G/GEJ AC cohort.
Measured: Up to 2 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted14 Jul 2022
- Study start26 Oct 2022
- Primary completion30 Jun 2027 (estimated)
- Study completion31 Dec 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Locally Advanced Unresectable or Metastatic Solid TumorsStudies of the same condition, open and under way.
- More trials run by Innovent Biologics (Suzhou) Co. Ltd.The sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 1
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 470 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Innovent Biologics (Suzhou) Co. Ltd.
- Sponsor type
- Industry (pharma, biotech, devices)
- Collaborators
- Fortvita Biologics (USA)Inc., TigerMed
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05458219
- Sponsor's protocol ID
- CIBI343A101
- Status last verified
- Apr 2026
- First submitted
- 11 Jul 2022
- Last updated
- 4 May 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Liu J, Yang J, Sun Y, Gong J, Yue J, Pan Y, Sun M, Song R, Xiao X, Tazbirkova A, Ruan J, Liu Z, Liu Z, Li Z, Sheng L, Qin Y, Ying J, Yu X, Zhang J, Mou Y, Lu C, Chen P, Li S, Li J, Qu X, Deng T, Du J, Zhou A, Li E, Yuan X, Liang X, Yu W, Morris M, Luo Y, Zhao X, Guo Y, Zhou H, Shen L. CLDN18.2-targeting antibody-drug conjugate IBI343 in advanced gastric or gastroesophageal junction adenocarcinoma: a phase 1 trial. Nat Med. 2025 Sep;31(9):3028-3036. doi: 10.1038/s41591-025-03783-8. Epub 2025 Jul 16.
PubMed 40670773