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NCT06433531Fut, nem toboroz1. fázis

A Clinical Study of TQH2929 Injection in Treatment With Generalized Pustular Psoriasis (GPP)

Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic Profile, and Efficacy of TQH2929 in Healthy Adult Subjects and Psoriasis Subjects

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2025. júl. 30.

Következő lépések

Rövid összefoglaló (regiszter, angolul)

This study is a multicenter, single-group, open-label study to evaluate the safety and tolerability of TQH2929 injection at a dose of 900mg in adult subjects with active Generalized Pustular Psoriasis (GPP), and to preliminarily evaluate the efficacy.

Állapot (regiszter)
Fut, nem toboroz
Fázis (regiszter)
1. fázis
Vizsgálattípus
Beavatkozással járó
Résztvevők száma
9 (tényleges)
Első benyújtás
2024. máj. 23.
Kezdés
2024. jún. 19.
Elsődleges befejezés
2025. júl. 8.
Fő szponzor
Chia Tai Tianqing Pharmaceutical Group Nanjing Shunxin Pharmaceutical Co., Ltd.
Betegségek
Pikkelysömör
NCT-szám
NCT06433531

Mit vállalsz

  • Vizsgálat típusa: Beavatkozással járó · 1. fázis
  • Bevont résztvevők: 9
  • 2024. jún. 19. és az elsődleges befejezés (2025. júl. 8.) között
  • 7 helyszín, 1 országban
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.

Ki nem vehet részt

Szó szerint a(z) ClinicalTrials.gov forrásból, témák szerint csoportosítva. Hogy ki vehet részt, azt csak a vizsgálat csapata dönti el.

Korábbi kezelés

  • Positive antibodies to treponema pallidum during screening;
  • History of serious infection leading to hospitalization or intravenous infusion of antibiotics or antiviral therapy within 3 months prior to baseline;
  • Active systemic infections requiring systemic antibiotics or systemic antiviral therapy within 4 weeks prior to baseline;
  • History of opportunistic infection and parasitic infection within 6 months prior to the screening period;
  • History of herpes zoster infection within 2 months prior to baseline;
  • Receive major surgery within 4 weeks prior to the first dose;
  • Use of the following medications within the prescribed time:
    • Receive topical drugs for the treatment of skin diseases within 1 weeks prior to baseline;
    • Receive systemic therapy within 4 weeks prior to baseline;
    • Receive regular phototherapy within 4 weeks prior to baseline;
    • Within 12 weeks prior to baseline, receive live (attenuated) vaccine;
    • Receive antibiotics and antivirals within 4 weeks prior to baseline.
  • People who are alcoholic, drug addicts, and known drug dependents;
  • Received a blood transfusion within 4 weeks prior to the first dose;
  • During the period of participation in this study, participants had planned surgical procedures;
  • Have participated in clinical trials of other drugs or medical devices within 4 weeks prior to baseline;

Más betegség

  • Computed Tomography of the chest shows active or occult tuberculosis or a history of contact with an open tuberculosis (TB) subject within the past 6 months. Subjects positive for tuber closes spot(T-SPOT) (or other tuberculosis diagnostic test) result;
  • Active hepatitis during the screening period, or positive for hepatitis B surface antigen (HBsAg);
  • History of human immunodeficiency virus (HIV) infection, or positive HIV serological results at screening during screening;
  • Subject has known or suspected autoimmune disease;
  • Subjects with any type of active malignancy or a history of malignancy (except cervical cancer or non-metastatic cutaneous squamous cell carcinoma, basal cell carcinoma and papillary thyroid carcinoma) that has been cured for more than 5 years prior to the screening period;
  • Subjects have history of significant drug allergies;
  • In the judgment of the investigator or sponsoring medical auditor, it is believed that there are any medical or psychiatric symptoms that put the subject at risk, interfere with participation in the study, or interfere with the interpretation of the results of the study.

Egyéb

  • Patients with primary plaque psoriasis vulgaris with pustules that are restricted to psoriatic plaques;
  • Immediate life-threatening flare of Generalized Pustular Psoriasis or requiring intensive care treatment, according, to the judgment of the investigator;
  • Pregnant or Breasting feeding subject;
  • Subject is unable to tolerate intravenous infusion administration;

Kiket keres a vizsgálat

  • Adults aged between 18 and 75 years (inclusive),both male and female;
  • A known and documented history of Generalized Pustular Psoriasis diagnosed with European Rare and Severe Psoriasis Expert Network (ERASPEN) criteria in 2017;
  • Presenting with a moderate-severe flare of Generalized Pustular Psoriasis (GPP)
  • Body mass index (BMI) within 18~36 kg/m2;
  • Major organ function is good;
  • Patients must be able to understand and sign a written informed consent document;
  • Patients must be able to complete study-related procedures and questionnaires;
  • Female and male subjects of childbearing age should agree to use contraceptive measures during the study period and within 6 months after the end of the study; Female subjects need to serum pregnancy pregnancy test within 7 days before study enrollment.

Életkor a regiszterben: 18 év – 75 év · Nem: nők és férfiak · Egészséges önkénteseket nem fogad

A teljes feltétellista: ClinicalTrials.gov

Helyszínek (7)

Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.

HelyszínVárosOrszágHelyszín állapota
Peking University First HospitalBeijingKínaIsmeretlen állapot
Second People's Hospital of ChengduChengduKínaIsmeretlen állapot
Dermatology Hospital of Southern Medical UniversityeGuangzhouKínaIsmeretlen állapot
The Second Affiliated Hospital Zhejiang University School of MedicineHangzhouKínaIsmeretlen állapot
The First Hospital of China Medical UniversityShenyangKínaIsmeretlen állapot
The Second Hospital of Hebei Medical UniversityShijiazhuangKínaIsmeretlen állapot
The First Hospital of Hebei Medical UniversityShijiazhuangKínaIsmeretlen állapot

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