- ICH GCP
- USA klinikai vizsgálatok nyilvántartása
- Klinikai vizsgálat NCT07589205
Study of IBI3028 in Participants With Locally Advanced, Unresectable, or Metastatic Solid Tumors
A Phase 1, Multi-Center, Open-Label Study Evaluating IBI3028 Treatment in Participants With Locally Advanced, Unresectable, or Metastatic Solid Tumors
A tanulmány áttekintése
Állapot
Körülmények
Beavatkozás / kezelés
Tanulmány típusa
Beiratkozás (Becsült)
Fázis
- 1. fázis
Kapcsolatok és helyek
Tanulmányi kapcsolat
- Név: Shijie Liu
- Telefonszám: (+86)18701121959
- E-mail: shijie.liu@innoventbio.com
Tanulmányi helyek
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Tianjin Municipality
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Tianjin, Tianjin Municipality, Kína, 300060
- Toborzás
- Tianjin Medical University Cancer Institute and Hospital
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Kutatásvezető:
- Yi Hu
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Kutatásvezető:
- Jihui Hao
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Kapcsolatba lépni:
- Jihui Hao
- Telefonszám: 18622221120
- E-mail: haojihui@tjmuch.com
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Részvételi kritériumok
Jogosultsági kritériumok
Tanulmányozható életkorok
- Felnőtt
- Idősebb felnőtt
Egészséges önkénteseket fogad
Leírás
Inclusion Criteria
- Be able to understand and sign written informed consent to participate in this study, including all assessments and procedures specified in this protocol;
- Male or female participants aged 18 years or older;
- Have histologically or cytologically confirmed unresectable locally advanced or metastatic solid tumors;
- Have at least one evaluable lesion (dose escalation) or measurable lesion (dose expansion) as per RECIST v1.1 within 28 days prior to the first dose of IBI3028;
- ECOG PS(Eastern Cooperative Oncology Group Performance Status)score of 0-1;
- Anticipated life expectancy of ≥ 12 weeks;
Adequate bone marrow and organ function as evidenced by :
- Hematological function: ANC(Absolute neutrophil count) ≥ 1.5 × 10 9 /L; platelet count (PLT) ≥ 90 × 10 9 /L; hemoglobin ≥ 9.0 g/dL, and without receiving granulocyte-colony stimulating factor (G-CSF), granulocyte-macrophage colony stimulating factor (GM-CSF), thrombopoietin (TPO), interleukin-11, or other leukocyte/platelet stimulating growth factors (including red blood cell and platelet transfusions) within at least 7 days before the first dose of the study drug;
- Hepatic function: total bilirubin ≤ 1.5 × ULN (Upper Limit of Normal) (≤ 3 × ULN for participants with Gilbert's syndrome); AST(Aspartate Aminotransferase) and ALT (Alanine Aminotransferase)≤ 2.5 × ULN in the absence of liver metastases (≤ 5 × ULN if liver metastases are present); albumin ≥ 2.8 g/dL;
- Renal function: creatinine clearance ≥ 30 mL/min (using Cockcroft-Gault formula); urine protein < 2+ or 24-h total urine protein < 1 g;
- Cardiac function: Left ventricular ejection fraction (LVEF) ≥ 50%, no clinically significant pericardial effusion as determined by ECHO or MUGA(Multigated Acquisition), and no clinically significant ECG result;
- Coagulation function: International normalized ratio (INR) ≤ 1.5; activated partial thromboplastin time (aPTT) ≤ 1.5 × ULN (participants receiving anticoagulant therapy with coagulation function within the range above are allowed);
- Pulmonary function: With at least the lowest level of pulmonary reserve, defined as Grade ≤ 1 dyspnea and blood oxygen saturation ≥ 95% in non-oxygen breathing state;
- Participants (both male and female participants) who will be not of childbearing potential or who agree to use at least 1 highly effective method of contraception during the study (from start of screening or within 2 weeks prior to first dose, whichever occurs first, and continue until 7 months for females and 4 months for males after the last dose of study drug).
Exclusion Criteria
- Participation in any other interventional clinical study other than an observational (non-interventional) study or during the follow-up period of an interventional study;
Prior anti-tumor therapy:
Participants who have received cytotoxic therapy within 3 weeks or 5 half-lives (whichever is shorter) prior to the first administration of study intervention ; Participants who have received PD-1/PD-L1 therapy within 4 weeks prior to the first administration of study drug; Participants who have received treatment with small molecule targeted therapy within 14 days or 5 half-lives (whichever is shorter) prior to the first dose of the study drug; Palliative radiation therapy within 2 weeks or radical radiation therapy within 4 weeks prior to the first dose of study drug; Participants who had received adoptive cell therapy within 8 weeks prior to the first administration of study intervention.
- Have received live vaccines within 4 weeks or tumor vaccines within 3 months prior to the first administration of the study drug, or plan to receive any live vaccines during the study;
- Use of strong cytochrome P450 3A4 (CYP3A4) enzyme inhibitors within 2 weeks or 5 half-lives (whichever is shorter) prior to the first dose of study drug;
- Adverse reactions caused by previous anti-tumor treatments that have not resolved to Grade 0 or 1 or baseline level according to NCI CTCAE v5.0 before the first dose of the study drug (except for alopecia, fatigue, pigmentation, and other conditions with no safety implications per the Investigator's clinical judgement);
- Known allergies, hypersensitivity, or intolerance to IBI3028 or its excipients (refer to the Investigator's Brochure);
- Have undergone major surgery (craniotomy, thoracotomy, or laparotomy, and other surgeries according to Investigators' opinion, excluding needle biopsy) within 4 weeks prior to the first dose of the investigational product, or are expected to undergo major surgery during the study, or have severe unhealed wounds, ulcers, etc.;
- Known symptomatic central nervous system (CNS) metastases. Participants with asymptomatic CNS metastases (ie, no neurologic syndrome and metastases ≤1.5 cm in diameter) or stable disease after treatment as judged by the investigator may be considered if: they have no metastases in the midbrain, pons, cerebellum, meninges, medulla oblongata, or spinal cord; stable status for at least 4 weeks prior to the first dose of study drug (≤1.5 mg/day dexamethasone or equivalent and baseline anticonvulsants are allowed), and have no new or enlarging CNS metastases as clearly demonstrated by clinical evidence; Note : CNS lesions are not considered target lesions.
Uncontrolled disease or condition, including:
- Uncontrolled infection requiring systemic antibiotics, antivirals, or antifungals prior to the first dose of the study drug;
- With known human immunodeficiency virus (HIV) infection, or HIV positive (HIV 1/2 Ab positive), for participants outside mainland China, participants with positive HIV antibody test at screening are eligible to participate in the study under the premise of undetectable viral load, or well-controlled under antiretroviral therapy (defined as CD4+ T cell count ≥ 350 cells/μL and no history of AIDS-defining opportunistic infection within 12 months before the first dose);
- Acute or chronic active hepatitis B (HBsAg positive and/or HBcAb positive, and HBV DNA titer ≥ 10 4 copies/mL or ≥ 2000 IU/mL) or hepatitis C (HCV Ab positive, and HCV RNA > 10 3 copies/mL or above the lower limit of detection);
- Active tuberculosis infection, or still receiving anti-tuberculosis treatment, or receiving anti-tuberculosis treatment within 1 year before the first dose of the study drug;
- Uncontrolled myocarditis or symptomatic congestive heart failure Class II-IV (New York Heart Association ,NYHA), symptomatic or uncontrolled arrhythmia, QTc interval > 480 ms, or personal or family history of congenital long/short QT syndrome;
- Uncontrolled hypertension with SBP ≥ 160 mmHg or DBP ≥ 100 mmHg measured on 2 follow-up visits despite adequate standard treatment;
- Current gastrointestinal tract (muscle-derived tube from the oral cavity to the anus, including oral cavity, pharynx, esophagus, stomach, duodenum, jejunum, ileum, cecum, appendix, colon, rectum, and anus) or endotracheal stent implantation;
- Significant malnutrition, such as malnutrition requiring parenteral nutrition;
- Spinal cord compression that has not been radically cured by surgery and/or radiotherapy;
- Ascites, pleural effusion, or pericardial effusion that is symptomatic and requires intervention prior to the first dose of study intervention (participants who do not require treatment or who recover steadily without intervention are eligible).
- With a history of pneumonia requiring corticosteroid treatment, or a history of clinically significant lung diseases (such as interstitial lung disease, non-infectious pneumonitis, or uncontrolled lung diseases such as pulmonary fibrosis, severe radiation pneumonitis, and acute lung injury), or suspected of having these diseases by imaging during the screening period;
- Any history of arterial thromboembolic events within 6 months prior to the first dose of the study drug, including myocardial infarction, unstable angina, cerebrovascular stroke, or transient ischemic attack;
- Esophageal or gastric varices requiring immediate intervention (e.g., ligature or sclerotherapy) or at high risk of bleeding according to the opinion of the investigator or a gastroenterologist or hepatologist. Participants with evidence of portal hypertension (including imaging findings of hypersplenism) or a history of esophageal and gastric variceal bleeding must undergo endoscopic evaluation within 3 months prior to the first dose of the study drug;
- Any history of life-threatening hemorrhage or hemorrhage requiring blood transfusion, endoscopy, or surgery within 3 months prior to the first dose of the investigational product ;
- Unhealed gastrointestinal obstruction, perforation, or fistula. At risk of gastrointestinal obstruction or perforation (including but not limited to: acute diverticulitis, abdominal abscess, etc.), history of extensive bowel resection (segmental colectomy or extensive bowel resection accompanied with chronic diarrhea), active inflammatory bowel disease, or Grade ≥ 2 chronic diarrhea;
- History of immunodeficiency diseases, including congenital or acquired immunodeficiency diseases;
- History of allogeneic organ transplantation or allogeneic bone marrow transplantation, or autologous hematopoietic stem cell transplantation within 3 months prior to the first dose of the investigational drug, except for corneal transplantation;
History of other malignancy within 2 years before the first dose of study drug(s), with the following exceptions:
- Malignancy (other than in situ) treated with curative therapy with no known active disease present for ≥ 2 years prior to the first dose of study drug and at low risk of recurrence according to the physician's opinion;
- Adequately treated non-melanoma skin cancer or lentigo maligna without evidence of residual or recurrent disease;
- Adequately treated carcinoma in situ without evidence of residual or recurrent disease;
- Prostate intraepithelial neoplasia without evidence of prostate cancer;
- Adequately treated urothelial papillary non-invasive carcinoma.
- Presence of any indwelling tubes or drains (such as percutaneous nephrostomy tubes, indwelling Foley catheters, biliary drainage tubes, or peritoneal/pericardial catheters); Note: Thoracic catheters or dedicated central venous access catheters such as Port-A-Cath or Hickman catheters are allowed.
- Other acute or chronic diseases or laboratory abnormalities, which may increase the risk of participating in the study or receiving the investigational product, interfere with the interpretation of study results, and make the participant unsuitable for participating in the study based on the investigator's judgment;
- Neurological, mental, or social conditions that affect the compliance with trial requirements, significantly increase the risk of AEs, or affect the participants' signing of written informed consent (IC);
- Females who are pregnant, have a positive pregnancy test result, or are breastfeeding;
- Not fit to participate in this study at the discretion of the Investigator.
Tanulási terv
Hogyan készül a tanulmány?
Tervezési részletek
- Elsődleges cél: Kezelés
- Kiosztás: N/A
- Beavatkozó modell: Szekvenciális hozzárendelés
- Maszkolás: Nincs (Open Label)
Fegyverek és beavatkozások
Résztvevő csoport / kar |
Beavatkozás / kezelés |
|---|---|
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Kísérleti: Drug: IBI3028
IBI3028 will be dosed until disease progression, toxicity intolerance, starting of new systemic anti-cancer treatment, withdrawal of consent, occurrence of other reasons for discontinuing study therapy, or treatment duration reaching the maximum of 24 months, whichever occurs first.
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Recombinant anti-EGFR(Epidermal growth factor receptor) and c-Met antibodies-dual-payload conjugate for injection
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Mit mér a tanulmány?
Elsődleges eredményintézkedések
Eredménymérő |
Intézkedés leírása |
Időkeret |
|---|---|---|
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Azon alanyok száma, akiknél a fizikális vizsgálat eredményeiben klinikailag jelentős változás következett be
Időkeret: Legfeljebb 3 év
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A vizsgáló által jelentett klinikailag jelentős kóros fizikális vizsgálati eredmények.
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Legfeljebb 3 év
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Azon alanyok száma, akiknél az elektrokardiogram klinikailag jelentős változásai voltak
Időkeret: Legfeljebb 3 év
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A vizsgáló által jelentett klinikailag jelentős kóros elektrokardiogram lelet.
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Legfeljebb 3 év
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Az a betegek száma, akik klinikailag szignifikáns változásokkal rendelkeznek az életképességben
Időkeret: Legfeljebb 3 év
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Vital jelek, beleértve a testhőmérsékletet, az impulzust, a légzési sebességet, az oxigén telítettségét pulzus -oximetriával nyugalomban és vérnyomáson
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Legfeljebb 3 év
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A dózis korlátozó toxicitások (DLT)
Időkeret: Legfeljebb 21 nap
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Dózis korlátozza a toxicitást (DLT) az MTD és/vagy az RP2D megállapításához.
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Legfeljebb 21 nap
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A laboratóriumi paraméterek klinikailag szignifikáns változásaival rendelkező betegek száma
Időkeret: Legfeljebb 3 év
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Klinikailag szignifikáns, rendellenes laboratóriumi paraméterek eredményei, amelyeket a vizsgáló jelentett.
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Legfeljebb 3 év
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Numbers of subjects with adverse events
Időkeret: Up to 3 years
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Defined as any untoward medical occurrence, whether or not there is a causal relationship with the study drug, in a clinical study subject from the time informed consent form is signed
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Up to 3 years
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Numbers of subjects with serious adverse events
Időkeret: Up to 3 years
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Defined as any serious untoward medical occurrence, whether or not there is a causal relationship with the study drug, in a clinical study subject from the time informed consent form is signed
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Up to 3 years
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Number of AEs(adverse events) leading to dose interruption
Időkeret: Up to 3 years
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AEs(adverse events) leading to dose interruption reported by the investigator
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Up to 3 years
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Number of AEs leading to dose reduction
Időkeret: Up to 3 years
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AEs leading to dose reduction reported by the investigator
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Up to 3 years
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Number of AEs leading to permanent discontinuation
Időkeret: Up to 3 years
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AEs leading to permanent discontinuation reported by the investigator
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Up to 3 years
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Objective response rate (ORR) in dose expansion
Időkeret: Up to 3 years
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Objective response rate (ORR) as evaluated per the RECIST v1.1 criteria.
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Up to 3 years
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Másodlagos eredményintézkedések
Eredménymérő |
Intézkedés leírása |
Időkeret |
|---|---|---|
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Area under the curve (AUC)
Időkeret: Up to 3 years
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Area under the curve (AUC) of single and multiple doses of IBI3028
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Up to 3 years
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Maximum concentration (Cmax)
Időkeret: Up to 3 years
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Maximum concentration (Cmax) of single and multiple doses of IBI3028
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Up to 3 years
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Time to maximum concentration (Tmax)
Időkeret: Up to 3 years
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Time to maximum concentration (Tmax) of single and multiple doses of IBI3028
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Up to 3 years
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Clearance (CL)
Időkeret: Up to 3 years
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Clearance (CL) of single and multiple doses of IBI3028
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Up to 3 years
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Apparent volume of distribution (V)
Időkeret: Up to 3 years
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apparent volume of distribution (V) of single and multiple doses of IBI3028
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Up to 3 years
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Half-life (t1/2)
Időkeret: Up to 3 years
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Half-life (t1/2) of IBI3020 to the last administration of IBI3028
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Up to 3 years
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Anti-drug antibody (ADA)
Időkeret: Up to 3 years
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Incidence and characterization of anti-drug antibody (ADA)
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Up to 3 years
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Neutralizing antibody (NAb)
Időkeret: Up to 3 years
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Incidence and characterization of neutralizing antibody (NAb)
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Up to 3 years
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Objective response rate (ORR)
Időkeret: Up to 3 years
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Objective response rate (ORR) as evaluated per the RECIST v1.1 criteria
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Up to 3 years
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Duration of response (DoR)
Időkeret: Up to 3 years
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Duration of response (DoR) as evaluated per the RECIST v1.1 criteria
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Up to 3 years
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Disease control rate (DCR)
Időkeret: Up to 3 years
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Disease control rate (DCR) as evaluated per the RECIST v1.1 criteria
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Up to 3 years
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Time to response (TTR)
Időkeret: Up to 3 years
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Time to response (TTR) as evaluated per the RECIST v1.1 criteria
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Up to 3 years
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Progression-free survival (PFS)
Időkeret: Up to 3 years
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progression-free survival (PFS) as evaluated per the RECIST v1.1 criteria
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Up to 3 years
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Overall survival (OS)
Időkeret: Up to 3 years
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OS is defined as the time from the date of first dose of study drug until the date of death from any cause.
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Up to 3 years
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Együttműködők és nyomozók
Tanulmányi rekorddátumok
Tanulmány főbb dátumok
Tanulmány kezdete (Tényleges)
Elsődleges befejezés (Becsült)
A tanulmány befejezése (Becsült)
Tanulmányi regisztráció dátumai
Először benyújtva
Először nyújtották be, amely megfelel a minőségbiztosítási kritériumoknak
Első közzététel (Tényleges)
Tanulmányi rekordok frissítései
Utolsó frissítés közzétéve (Tényleges)
Az utolsó frissítés elküldve, amely megfelel a minőségbiztosítási kritériumoknak
Utolsó ellenőrzés
Több információ
A tanulmányhoz kapcsolódó kifejezések
További vonatkozó MeSH feltételek
- Neoplazmák webhelyenként
- Neoplazmák
- Bélbetegségek
- Légúti betegségek
- Neoplazmák szövettani típus szerint
- Gasztrointesztinális neoplazmák
- Emésztőrendszeri neoplazmák
- Emésztőrendszeri betegségek
- Emésztőrendszeri betegségek
- Bél neoplazmák
- Rektális betegségek
- Tüdőbetegségek
- A fej és a nyak daganatai
- Neoplazmák, mirigyes és epiteliális
- Légúti neoplazmák
- Mellkasi neoplazmák
- Vastagbélbetegségek
- Tüdő neoplazmák
- Karcinóma
- Karcinóma, bronchogén
- Bronchiális neoplazmák
- Karcinóma, laphámsejtes
- A fej és a nyak laphámsejtes karcinóma
- Kolorektális neoplazmák
- Karcinóma, nem kissejtes tüdő
Egyéb vizsgálati azonosító számok
- CIBI3028A101
Gyógyszer- és eszközinformációk, tanulmányi dokumentumok
Egy amerikai FDA által szabályozott gyógyszerkészítményt tanulmányoz
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