Phase I Trial of Subcutaneous VDJ010 In Healthy Subjects and Patients With Ulcerative Colitis
A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase I Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single and Multiple Ascending Doses of VDJ010 for Subcutaneous Injection in Healthy Chinese Subjects and Patients With Ulcerative Colitis
This study adopted a multi-center, randomized, double-blind, placebo-controlled, single- and multiple-ascending dose design, using recombinant human IL-2 fusion protein (VDJ010) administered subcutaneously to evaluate its safety, tolerability, pharmacokinetics, and pharmacodynamics in healthy Chinese subjects and patients with ulcerative colitis.
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Detaljeret beskrivelse
This study is a first-in-human, Phase I, multi-center, double-blind, placebo-controlled, single- and multiple-ascending dose trial designed to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of subcutaneously administered VDJ010 (recombinant human fusion protein) in two parts: Part A enrolls 28 healthy subjects across four single-dose cohorts (500K, 750K, 1,000K, and 1,250/1,500K IU), and Part B enrolls 20 patients with moderately to severely active ulcerative colitis across three multiple-dose cohorts (750K, 1,000K, and 1,250/1,500K IU) dosed subcutaneously every two weeks for a total of three doses. The primary objective is to assess safety and tolerability, while secondary objectives include characterizing PK profiles, immunogenicity (ADA/NAB), and PD effects measured by changes in peripheral blood Treg, Tcon, NK, and B cell subsets. Exploratory efficacy endpoints in UC patients include clinical response and remission rates based on modified Mayo score, endoscopic remission, UCEIS score, IBDQ quality of life, and biomarkers such as CRP and fecal calprotectin at Week 8. Dose escalation follows predefined safety stopping criteria with review intervals between cohorts, and all safety assessments are conducted per CTCAE V6.0 through 43 days (healthy) or 57 days (UC) of follow-up.
Undersøgelsestype
Undersøgelsestype
Tilmelding (Anslået)
Tilmelding
Fase
Fase
- Fase 1
Kontakter og lokationer
Studiesteder
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Anhui
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Hefei, Anhui, Kina
- Ikke rekrutterer endnu
- The First Affiliated Hospital of Anhui Medical University
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Kontakt:
- Juan Wu
- Telefonnummer: +86-13956038063
- E-mail: julianwu871109@sina.com
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Beijing Municipality
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Beijing, Beijing Municipality, Kina
- Rekruttering
- Peking Union Medical College Hospital
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Kontakt:
- Hong Yang
- Telefonnummer: +86-13811790704
- E-mail: hongy72@163.com
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Kontakt:
- Rui Chen
- Telefonnummer: +86-13811790704
- E-mail: chenrui04@126.com
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Fujian
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Xiamen, Fujian, Kina
- Ikke rekrutterer endnu
- Xiamen Hospital of Traditional Chinese Medicine
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Kontakt:
- Bin Zhao
- Telefonnummer: +86-13810698675
- E-mail: zjx@vdjbio.com
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Hebei
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Shijiazhuang, Hebei, Kina
- Ikke rekrutterer endnu
- The Second Hospital of Hebei Medical University
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Kontakt:
- Xiaolan Zhang
- Telefonnummer: +86-15803212979
- E-mail: xiaolanzh@126.com
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Shaanxi
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Xi'an, Shaanxi, Kina
- Ikke rekrutterer endnu
- The Second Affiliated Hospital of Xi'an Jiaotong University
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Kontakt:
- Yan Cheng
- Telefonnummer: +86-15129085363
- E-mail: drchengyan@163.com
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Shanxi
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Taiyuan, Shanxi, Kina
- Ikke rekrutterer endnu
- The First Hospital of Shanxi Medical University
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Kontakt:
- Linglin Tian
- Telefonnummer: +86-13935192515
- E-mail: tianlinlin587@163.com
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Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
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Healthy Subjects:
- Signed informed consent form and able to comply with the study protocol.
- Age ≥ 18 and ≤ 55 years (on the date of signing ICF); body weight ≥ 45.0 kg for women and ≥ 50.0 kg for men; BMI 18.0-28.0 kg/m² (inclusive).
- Normal function of major organs (heart, lung, liver, kidney).
- Negative serum pregnancy test for women of childbearing potential; willingness to use adequate contraceptive methods (e.g., abstinence, IUD, condoms) during the study and for 6 months after dosing.
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UC Patients:
- Age ≥ 18 and ≤ 75 years (on the date of signing ICF); male and female.
- Confirmed diagnosis of ulcerative colitis for ≥ 3 months prior to screening, per Chinese UC Diagnostic and Treatment Guidelines (2023, Xi'an), confirmed by endoscopy and histology within 14 days prior to randomization.
- Active UC defined as modified Mayo score ≥ 4 and ≤ 9, with stool frequency subscore ≥ 1, rectal bleeding subscore ≥ 1, and endoscopic subscore ≥ 2 (colonoscopy within 14 days acceptable).
- If UC history > 10 years, documented colonoscopy within 12 months prior to screening (or at screening). Those with family history of CRC, age > 50, or high-risk factors per investigator must have up-to-date CRC screening results.
- Negative serum pregnancy test for women of childbearing potential; male and female participants with reproductive potential must agree to use acceptable contraception during treatment and for 6 months after last dose.
- UC inflammation confirmed to extend proximal to the rectum, beyond the rectosigmoid junction (≥ 15 cm from anal verge) by colonoscopy.
- Voluntary participation with signed ICF.
- For patients on baseline UC therapies, the following washout/stability requirements must be met prior to randomization:
Oral 5-ASA agents: stable dose ≥ 2 weeks; Oral corticosteroids (prednisolone ≤ 25 mg/day or equivalent): stable dose ≥ 2 weeks Oral budesonide (≤ 9 mg/day): stable dose ≥ 2 weeks; Oral immunomodulators (MTX, AZA, 6-MP): stable dose ≥ 12 weeks
Exclusion Criteria:
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Healthy Subjects:
- Allergic constitution (allergy to two or more drugs/foods).
- History of malignancy, neurological or psychiatric disorders (including epilepsy or dementia), heart failure, immunodeficiency, immunosuppressive disease, or IBD; or major surgery within 6 months prior to randomization.
- Severe bleeding tendency affecting venous access, or unable/unwilling to undergo venipuncture.
- Vaccination within 1 month prior to randomization.
- Prior treatment with anti-IL-2 or IL-2 receptor-targeted therapy; use of any biologic agent within 6 months prior to randomization or currently.
- Participation in another clinical trial with drug administration within 3 months prior to randomization.
- Blood donation (whole blood or components) or significant blood loss (≥ 400 mL) within 3 months prior to randomization.
- Active bacterial, viral, fungal, or parasitic infection, or any infection requiring systemic anti-infective therapy within 4 weeks prior to randomization.
- Use of any medication (e.g., warfarin, cyclosporine, theophylline, simvastatin, omeprazole, dextromethorphan, Chinese patent medicine) or health supplements (vitamins, dietary supplements) within 2 weeks, or prescription medication within 1 month prior to randomization.
- History of drug abuse within 1 year or positive urine drug screen.
- Alcoholism or regular alcohol consumption > 14 units/week within 3 months (1 unit = 360 mL beer or 45 mL 40% spirit or 150 mL wine); positive alcohol breath test.
- Average daily smoking > 5 cigarettes within 3 months prior to first dose, or unable to abstain from tobacco during the study.
- Excessive daily consumption of tea, coffee, or caffeinated beverages (> 8 cups/day, 1 cup = 250 mL).
- Clinically significant abnormal findings on comprehensive physical examination, including: abnormal vital signs; clinically significant abnormal lab tests (hematology, urinalysis, liver function, renal function, coagulation), with mandatory exclusions for ANC ≤ 1.5×10⁹/L, platelet count ≤ 100×10⁹/L, AST or ALT > 2×ULN; clinically significant ECG abnormalities, PR ≥ 210 ms, QRS ≥ 120 ms, QTcF ≥ 450 ms.
- Positive T-SPOT.TB (may accept up to 2-fold ULN if no TB history and no symptoms).
- Positive for HIV-Ab, TP-Ab, HCV-Ab, or HBsAg.
- Clinically significant abnormal findings for RF, anti-dsDNA, ANA, or anti-CCP.
- Planned surgery (including cosmetic, dental, or oral surgery) or planned vigorous physical activity (including contact or collision sports) during the study.
- Planned blood donation during the study; planned receipt of any biologic agent within 3 months after study drug administration.
- Any condition that, in the investigator's judgment, makes the subject unsuitable for or unable to complete the study.
- Female-specific exclusions:
Oral contraceptive use within 30 days or planned during study; Long-acting estrogen/progestin injection, contraceptive patch, vaginal ring, subcutaneous implant, or contraceptive injection within 6 months; Unprotected intercourse within 14 days prior to randomization; Pregnancy or lactation; Plans for pregnancy, sperm/egg donation during the study or within 3 months after study completion
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UC Patients
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Crohn's disease (CD) or indeterminate colitis (IBD-U).
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Toxic megacolon, massive hemorrhage, perforation, sepsis, or intra-abdominal/peri-anal abscess requiring immediate surgical, endoscopic, or interventional treatment.
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History of ileostomy, proctocolectomy, or subtotal colectomy with ileorectal anastomosis.
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History of colorectal cancer, current CRC, serrated polyp with dysplasia, or atypical hyperplasia.
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Positive stool culture for pathogens or positive Clostridium difficile at screening. May be re-screened after adequate treatment and 30-day antibiotic washout.
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Clinically significant active infection; positive for HIV-Ab, TP-Ab, HCV-Ab, HBsAg (if HBsAg-negative but HBcAb-positive, add HBV-DNA; exclude if HBV-DNA > LLN), EBV-DNA, or CMV-DNA.
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Eosinophil count ≥ 2×ULN or diagnosed eosinophilia (including hereditary, primary, idiopathic, or secondary).
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Significant laboratory abnormalities:
Hb < 80 g/L; WBC < 2.5×10⁹/L; Platelets < 100×10⁹/L; Clinically significant ECG abnormalities: PR ≥ 210 ms, QRS ≥ 120 ms, QTcF < 350 ms or ≥ 450 ms (Fridericia correction); Creatinine ≥ 1.5×ULN; Total bilirubin > 34.2 μmol/L; ALT or AST > 2×ULN; GGT > 2×ULN; Abnormal thyroid function (hyper- or hypothyroidism)
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Positive T-SPOT.TB.
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Receipt of another investigational drug within 5 half-lives prior to planned first SC dose.
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History of malignancy within 5 years.
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Uncontrolled angina or symptomatic congestive heart failure (NYHA class III or IV).
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Allergy to any component of the study drug.
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Pregnancy or lactation.
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Prior treatment with IL-2 class drugs; use of biologics or small molecules (e.g., anti-TNF, anti-IL-12/23, IL-23 inhibitors, vedolizumab, JAK inhibitors, S1P receptor modulators) within 8 weeks or 5 half-lives (whichever longer) prior to baseline; cyclosporine or tacrolimus within 2 weeks; rectal formulations planned during study; Chinese herbal medicine for UC within 2 weeks prior to baseline.
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Unable to comply with study protocol or withdraws informed consent.
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Other conditions unsuitable for participation per investigator's judgment.
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Receipt of any live vaccine within 2 months prior to screening, BCG within 12 months, or planned live vaccination during the study.
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Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Firedobbelt
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
|---|---|
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Placebo komparator: Placebo
|
This is a matching placebo formulation containing no active pharmaceutical ingredient (API). The placebo is manufactured to be identical in appearance, color, shape, size, and packaging to the investigational product VDJ010 to maintain the integrity of the double-blind design. It is utilized solely as a control intervention for the purpose of this randomized, double-blind, placebo-controlled Phase I clinical trial. |
|
Eksperimentel: Recombinant human interleukin-2 fusion protein with human serum albumin (VDJ010) Injection
|
VDJ010 is a recombinant fusion protein consisting of human interleukin-2 (IL-2) genetically fused to human serum albumin (HSA), produced using Chinese hamster ovary (CHO) cells through DNA recombinant technology. The fusion protein selectively binds to the high-affinity IL-2 receptor (IL-2Rαβγ) constitutively expressed on regulatory T cells (Treg), thereby promoting Treg expansion and restoring immune tolerance in autoimmune diseases such as ulcerative colitis. The HSA moiety extends the plasma half-life of IL-2 to enable less frequent subcutaneous dosing. |
Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Safety and tolerability
Tidsramme: First dose up to last follow-up visit (Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration)
|
Incidence and severity of adverse events |
First dose up to last follow-up visit (Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration)
|
|
Peak Serum Concentration (Cmax)
Tidsramme: Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration.
|
VDJ010 Cmax; assessed in healthy subjects (single dose) and UC patients (multiple-dose steady-state, Cmax,ss) |
Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration.
|
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Time to Peak Concentration (Tmax)
Tidsramme: Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration.
|
VDJ010 Tmax; assessed in healthy subjects (single dose) and UC patients (multiple-dose steady-state, Tmax,ss) |
Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration.
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Area Under the Serum Concentration-Time Curve from Time Zero to Last Quantifiable Concentration (AUC0-t)
Tidsramme: Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
VDJ010 AUC0-t; assessed in healthy subjects (single dose) and UC patients (multiple-dose steady-state, AUC0-t,ss) |
Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
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Area Under the Serum Concentration-Time Curve from Time Zero to Infinity (AUC0-∞)
Tidsramme: Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
VDJ010 AUC0-∞; assessed in healthy subjects (single dose) and UC patients (multiple-dose steady-state, AUC0-∞,ss) |
Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
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Terminal Elimination Rate Constant (λz)
Tidsramme: Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
VDJ010 λz; assessed in healthy subjects (single dose) and UC patients (multiple-dose steady-state) |
Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
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Terminal Elimination Half-Life (t1/2z)
Tidsramme: Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
VDJ010 t1/2z; assessed in healthy subjects (single dose) and UC patients (multiple-dose steady-state) |
Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
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Clearance (CLz)
Tidsramme: Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
VDJ010 CLz; assessed in healthy subjects (single dose) |
Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
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Trough Concentration at Steady State (Cmin,ss / Ctrough,ss)
Tidsramme: Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
VDJ010 Cmin,ss (Ctrough,ss); assessed in UC patients at steady state |
Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
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Area Under the Curve over One Dosing Interval at Steady State (AUC0-τ,ss)
Tidsramme: Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
VDJ010 AUC0-τ,ss; assessed in UC patients at steady state |
Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
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Average Concentration at Steady State (Cav,ss)
Tidsramme: Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
VDJ010 Cav,ss; assessed in UC patients at steady state |
Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
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Degree of Fluctuation (DF)
Tidsramme: Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
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VDJ010 degree of fluctuation (DF); assessed in UC patients at steady state |
Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
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Swing
Tidsramme: Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
VDJ010 Swing; assessed in UC patients at steady state. |
Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
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Apparent Volume of Distribution at Steady State (Vss/F)
Tidsramme: Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
VDJ010 Vss/F; assessed in UC patients at steady state |
Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
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Apparent Clearance at Steady State (CLss/F)
Tidsramme: Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
VDJ010 CLss/F; assessed in UC patients at steady state |
Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
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Percentage of AUC Extrapolated to Infinity (AUC_%Extrap)
Tidsramme: Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
Percentage of AUC extrapolated to infinity (AUC_%Extrap); assessed in healthy subjects (single dose) and UC patients (multiple-dose steady-state) |
Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
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Mean Residence Time to Infinity (MRT0-∞)
Tidsramme: Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
VDJ010 MRT0-∞; assessed in healthy subjects (single dose) and UC patients (multiple-dose steady-state) |
Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
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Accumulation Ratio Based on Cmax (Ra(Cmax))
Tidsramme: Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
VDJ010 accumulation ratio based on Cmax (Ra(Cmax)); assessed in UC patients |
Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
|
Accumulation Ratio Based on AUC (Ra(AUC))
Tidsramme: Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
VDJ010 accumulation ratio based on AUC (Ra(AUC)); assessed in UC patients |
Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
|
Immunogenicity
Tidsramme: Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
ADA and NAb incidence and percentage of positive ADA/NAB subjects; ADA titers; time from dosing to first ADA-positive result. |
Healthy Subjects: 43 days after administration; UC Patients: 57 days after administration
|
Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Pharmacodynamics
Tidsramme: Healthy Subjects: Pre-dose to D20; UC Patients: Pre-dose to D43.
|
Changes from baseline in the percentages of peripheral blood Treg, Tcon, NK, and B cells. |
Healthy Subjects: Pre-dose to D20; UC Patients: Pre-dose to D43.
|
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The modified Mayo score
Tidsramme: First dose up to last follow-up visit (Day1-Day57)
|
Percentage of participants achieving clinical remission, clinical response, endoscopic remission, and mucosal healing at Week 8, as defined by the modified Mayo score (based on screening values). |
First dose up to last follow-up visit (Day1-Day57)
|
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The modified Mayo score
Tidsramme: First dose up to last follow-up visit (Day1-Day57)
|
Changes from baseline in the modified Mayo score at Week 8. |
First dose up to last follow-up visit (Day1-Day57)
|
|
The endoscopic subscore
Tidsramme: First dose up to last follow-up visit (Day1-Day57)
|
Changes from baseline in the endoscopic subscore at Week 8. |
First dose up to last follow-up visit (Day1-Day57)
|
|
The Ulcerative Colitis Endoscopic Index of Severity (UCEIS)
Tidsramme: First dose up to last follow-up visit (Day1-Day57)
|
Changes from baseline in the UCEIS at Week 8. |
First dose up to last follow-up visit (Day1-Day57)
|
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The partial modified Mayo score (excluding endoscopy)
Tidsramme: First dose up to last follow-up visit (Day1-Day57)
|
Percentage of participants achieving symptom relief based on the partial modified Mayo score (excluding endoscopy) at Weeks 1, 2, 4, 6, and 8. |
First dose up to last follow-up visit (Day1-Day57)
|
|
The Bowel Disease Questionnaire (IBDQ) score
Tidsramme: First dose up to last follow-up visit (Day1-Day57)
|
Changes from baseline in IBDQ score at Weeks 2, 4, 6, and 8. |
First dose up to last follow-up visit (Day1-Day57)
|
|
C-reactive protein (CRP)/high-sensitivity CRP (hs-CRP)
Tidsramme: First dose up to last follow-up visit (Day1-Day57)
|
Changes from baseline in CRP/hs-CRP and FC at Weeks 1, 2, 4, 6, and 8. |
First dose up to last follow-up visit (Day1-Day57)
|
|
Fecal calprotectin (FC)
Tidsramme: First dose up to last follow-up visit (Day1-Day57)
|
Changes from baseline in CRP/hs-CRP and FC at Weeks 1, 2, 4, 6, and 8. |
First dose up to last follow-up visit (Day1-Day57)
|
Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Studiestart
Primær færdiggørelse (Anslået)
Primær færdiggørelse
Studieafslutning (Anslået)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- VDJ010-UC-I
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
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