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A Study of HS269 in Patients With Advanced Solid Tumors

24 september 2021 bijgewerkt door: Zhejiang Hisun Pharmaceutical Co. Ltd.

A Phase I, Open-label,Dose-escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Efficacy of HS269, in Patients With Advanced Solid Tumor

This is a Phase I, open-label, first in human study of HS269 tablet, a small molecule highly-selective RET Inhibitor. The dose-escalation study will assess the safety, tolerability, and pharmacokinetics of HS269 and determine the dose and schedule to be used in Phase II. Seventeen to thirty-six patients with advanced solid tumor may be enrolled in this study.

Studie Overzicht

Toestand

Nog niet aan het werven

Interventie / Behandeling

Studietype

Ingrijpend

Inschrijving (Verwacht)

36

Fase

  • Fase 1

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studiecontact

Studie Locaties

      • Shanghai, China
        • Shanghai Pulmonary Hospital
        • Contact:
          • Caicun Zhou

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar en ouder (Volwassen, Oudere volwassene)

Accepteert gezonde vrijwilligers

Nee

Geslachten die in aanmerking komen voor studie

Allemaal

Beschrijving

Inclusion Criteria:

  1. ≥18 years, no gender limit.
  2. Patients with advanced solid tumors confirmed by histology or cytology fail to receive standard treatment, or there is no standard treatment, or standard treatment is not applicable at this stage.
  3. At least one evaluable tumor lesion according to RECIST version 1.1.
  4. ECOG≤ 1.
  5. The estimated survival time was more than 3 months.
  6. The function of all organs was good, the specific indexes were as follows:

    Blood system (no transfusion or hematopoietic stimulating factor treatment within 14 days) i. #NEUT ≥1.5×109/L ii. PLT ≥90×109/L iii. HGB ≥85g/L Liver function i. TBIL ≤1.5×ULN ii. ALT ≤3×ULN; Patients with liver metastasis or liver cancer: ≤ 5 × ULN iii. AST ≤3×ULN; Patients with liver metastasis or liver cancer: ≤ 5 × ULN Renal function i. Ccr >50 ml/min(According to Cockcroft-Gault formula) Blood coagulation function i. APTT ≤1.5×ULN ii. INR ≤1.5×ULN

  7. The subjects should be informed and agreed to the study before the start of the trial, and sign the written informed consent voluntarily.

Exclusion Criteria:

  1. Received anti-tumor treatments within 14 days or less than 5 half-lives (whichever is longer) before the first use of the study drug
  2. Received blood transfusion, erythropoietin, recombinant human thrombopoietin or colony stimulating factor and other treatments within 7 days before receiving blood system examination during the screening period.
  3. Received other unmarketed clinical study drugs or treatments within 4 weeks before the first use of the study drug.
  4. Major organ surgery (excluding biopsy) or significant trauma occurred within 4 weeks before the first use of the study drug;
  5. Systemic administration of glucocorticoids (prednisone > 10 mg / day or equivalent dose of the same drug) or other immunosuppressants within 14 days before the first use of the study drug; except for local, eye, intra articular, nasal and inhaled corticosteroids; short-term use of glucocorticoids for preventive treatment (e.g. prevention of contrast agent allergy);
  6. CYP1A2/P-gp potent inhibitors or potent inducers were used within 7 days before the first use of the study drug;
  7. Resistance to selective RET inhibitors;
  8. The adverse reactions of previous anti-tumor therapy have not yet recovered to CTCAE 5.0 grade evaluation ≤ 1 (except for the toxicity without safety risk judged by researchers such as alopecia);
  9. Patients with central nervous system metastasis or meningeal metastasis with clinical symptoms, or other evidence indicating that the central nervous system metastasis or meningeal metastasis has not been controlled, which is not suitable for the study.
  10. Have active infection and need systemic anti infection therapy;
  11. Have a history of immunodeficiency, including HIV antibody test positive;
  12. Active hepatitis B, allowing preventive antiviral treatment other than interferon; hepatitis C virus infection;
  13. Present or past interstitial lung disease (except radiation-induced pulmonary fibrosis without hormone therapy);
  14. Poorly controlled diabetic patients.
  15. Have a history of serious cardiovascular and cerebrovascular diseases, including but not limited to:

    1. Serious abnormal cardiac rhythm or conduction, such as ventricular arrhythmia, Ⅱ - Ⅲ degree atrioventricular block, etc;
    2. In the resting state, average QTcF≥480ms in 12 lead -ECG;
    3. Acute coronary syndrome, congestive heart failure, aortic dissection, stroke or other cardiovascular events of grade 3 or above occurred within 6 months before the first administration;
    4. NYHA ≥II or LVEF<50%;
    5. Hypertension beyond clinical control;
  16. Could not take medication orally,or have severe gastrointestinal obstruction (such as gastrointestinal obstruction, gastrointestinal absorption);
  17. The third space effusion, which could not be controlled clinically, was not suitable for the study;
  18. Mental disorder or poor compliance;
  19. Eligible patients with fertility (male and female) do not agree to use reliable contraceptive methods (abstinence, condom, intrauterine device or ligation) with their partner during the trial and for at least 3 months after the last medication.
  20. Female patients have a positive blood pregnancy test within 7 days before enrollment, or breastfeeding women;
  21. The subjects were not suitable for the clinical study because of other serious systemic diseases or other reasons according to the investigator 's judgment.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: NVT
  • Interventioneel model: Opdracht voor een enkele groep
  • Masker: Geen (open label)

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Experimenteel: HS269
Multiple doses of HS269 tablets
Oral tablets, once daily. Dose escalation from 50 mg QD, through 100 mg, 200mg, 300 mg, 400 mg, to 500mg.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Dose limiting toxicities (DLT)
Tijdsspanne: From date of initial dose until up to 33 days for treatment
Incidence rate of dose limiting toxicities (DLT)
From date of initial dose until up to 33 days for treatment
Adverse Event(s) and Serious Adverse Event(s)
Tijdsspanne: Through study completion or early study discontinuation(up to 12 months)
The occurrence and rate of AE and SAE
Through study completion or early study discontinuation(up to 12 months)

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Peak Plasma Concentration (Cmax)
Tijdsspanne: From date of initial dose until up to 33 days for treatment
Cmax of HS269
From date of initial dose until up to 33 days for treatment
Area Under the Plasma Concentration versus Time Curve (AUC)
Tijdsspanne: From date of initial dose until up to 33 days for treatment
AUC of HS269
From date of initial dose until up to 33 days for treatment
Calcitonin in Peripheral Blood
Tijdsspanne: Through study completion or early study discontinuation(up to 12 months)
For Medullary Thyroid Cancer patients
Through study completion or early study discontinuation(up to 12 months)
Thyroglobulin in Peripheral Blood
Tijdsspanne: Through study completion or early study discontinuation(up to 12 months)
For non-MTC thyroid cancer patients
Through study completion or early study discontinuation(up to 12 months)
ORR
Tijdsspanne: Approximately 12 months
Objective response rate (ORR)
Approximately 12 months
DCR
Tijdsspanne: Approximately 12 months
Disease control rate (DCR)
Approximately 12 months
PFS
Tijdsspanne: Approximately 12 months
Progression free survival (PFS)
Approximately 12 months
Peripheral blood ctDNA
Tijdsspanne: Through study completion or early study discontinuation(up to 12 months)
Only for patients with positive RET gene mutation
Through study completion or early study discontinuation(up to 12 months)

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Onderzoekers

  • Hoofdonderzoeker: Qiming Wang, Henan Provincial Cancer Hospital
  • Hoofdonderzoeker: Qi Dang, Shandong Cancer Hospital

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Verwacht)

1 oktober 2021

Primaire voltooiing (Verwacht)

1 oktober 2022

Studie voltooiing (Verwacht)

1 april 2023

Studieregistratiedata

Eerst ingediend

2 september 2021

Eerst ingediend dat voldeed aan de QC-criteria

24 september 2021

Eerst geplaatst (Werkelijk)

27 september 2021

Updates van studierecords

Laatste update geplaatst (Werkelijk)

27 september 2021

Laatste update ingediend die voldeed aan QC-criteria

24 september 2021

Laatst geverifieerd

1 september 2021

Meer informatie

Termen gerelateerd aan deze studie

Aanvullende relevante MeSH-voorwaarden

Andere studie-ID-nummers

  • HS269-Ⅰ-01

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

Onbeslist

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

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