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A Clinical Study of MHB034C for Injection in Participants With Advanced Solid Tumors

4 november 2026 bijgewerkt door: Minghui Pharmaceutical (Shanghai) LTD

A Phase I/II Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Efficacy of MHB034C for Injection in Participants With Advanced Solid Tumors

This study is an open-label, multicenter, first-in-human (FIH) Phase I/II clinical study to evaluate the safety, tolerability, pharmacokinetic (PK) profile, and preliminary efficacy of MHB034C in participants with advanced solid tumors.

Studie Overzicht

Toestand

Nog niet aan het werven

Interventie / Behandeling

Gedetailleerde beschrijving

The phaseI/II study consists of two stages: a dose escalation stage and a dose expansion stage. The primary objective of the Phase I dose escalation stage is to evaluate the safety and tolerability of MHB034C in participants with advanced solid tumors; the primary objective of the Phase II dose expansion stage is to evaluate the antitumor efficacy of MHB034C in selected participants with advanced solid tumors.

Studietype

Ingrijpend

Inschrijving (Geschat)

400

Fase

  • Fase 2
  • 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 Municipality
      • Shanghai, Shanghai Municipality, China, 201419
        • Fudan University Shanghai Cancer Center
        • Contact:
          • Ethics Committee
          • Telefoonnummer: 85033 +86 021-64175590
          • E-mail: JJYIN555@163.com

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. Participants voluntarily agree to participate in this study and sign the informed consent form.
  2. Aged ≥ 18 years, regardless of sex.
  3. ECOG Performance Status (PS) score of 0-1.
  4. Life expectancy of more than 3 months.
  5. Female participants of childbearing potential, and male participants whose partners are women of childbearing potential, must agree to use highly effective contraception with their partners; must refrain from donating gametes, from initiating gamete cryopreservation, and from retrieving or using their own previously cryopreserved gametes for conception. Female participants of childbearing potential must have a negative serum β-HCG pregnancy test within 7 days prior to the first use of the investigational medicinal product (IMP), and must not be lactating.
  6. Ability to understand the study requirements and willingness and ability to comply with the study and follow-up procedures.
  7. Participants enrolled in the Phase I dose escalation stage must have advanced solid tumors confirmed by histopathological or cytological examination, and must have progressed on or been intolerant to standard therapy, or have no standard treatment available.
  8. Participants enrolled in the Phase II dose expansion stage must have advanced solid tumors confirmed by histopathological or cytological examination, and must have progressed on or been intolerant to standard therapy, or have no standard treatment available.
  9. During the dose escalation stage, the investigator should make best efforts to obtain consent from participants to provide pre-treatment tumor tissue samples; during the dose expansion stage, participants must agree to provide pre-treatment tumor tissue samples, and if such samples cannot be provided, enrolment is permitted only with the sponsor's approval.
  10. At least one measurable tumor lesion according to the RECIST v1.1 criteria.
  11. Adequate bone marrow function.
  12. Adequate hepatic function.
  13. Adequate renal function.
  14. Adequate coagulation function.
  15. Adequate cardiac function.

Exclusion Criteria:

  1. Has had another primary malignancy within 3 years prior to signing the informed consent form, excluding early-stage malignancies that have been curatively treated.
  2. Has previously used or is currently using an antibody-drug conjugate (ADC) with a topoisomerase I inhibitor as the payload, with certain exceptions.
  3. Has previously received doxorubicin at a cumulative dose of > 360 mg/m² or an equivalent dose of a similar agent.
  4. Has received chemotherapy or endocrine therapy within 3 weeks, or radiotherapy, biological therapy, immunotherapy, or other anti-tumor therapy within 4 weeks, prior to the first dose of the investigational medicinal product .
  5. Has spinal cord compression, leptomeningeal metastasis, brainstem metastasis, or unstable brain metastasis.
  6. Adverse events from prior anti-tumor therapy have not resolved to ≤ Grade 1 as assessed by NCI-CTCAE v6.0.
  7. Has undergone major surgery on a major organ (excluding biopsy) or experienced significant trauma within 4 weeks prior to the first use of the IMP, or requires elective surgery during the study period, or currently has severe unhealed or dehiscent wounds, active and clinically significant ulcers, untreated fractures, or active unhealed stomatitis.
  8. Has received a live vaccine or live attenuated vaccine within 4 weeks prior to the first use of the IMP.
  9. Has received or requires systemic corticosteroids or other immunosuppressive therapy within 14 days prior to the first use of the IMP, excluding topical, ophthalmic, intra-articular, intranasal, and inhaled corticosteroid therapy, and short-term corticosteroid use for prophylaxis.
  10. Has moderate or severe pulmonary disease that significantly impairs pulmonary function.
  11. Has a history of interstitial lung disease/pneumonitis (ILD), currently has ILD, or suspected ILD that cannot be ruled out by imaging during screening.
  12. Has severe cardiovascular disease or high-risk factors.
  13. Has experienced an arterial/venous thrombotic event within 6 months prior to the first dose.
  14. Has a clinically evident or uncontrolled third-space fluid collection requiring repeated drainage.
  15. Currently has an active autoimmune disease, or has a history of active autoimmune disease requiring systemic immunosuppressive therapy within 2 years prior to the first use of the IMP.
  16. Has clinically significant corneal disease, or is currently using other medications that may cause corneal damage.
  17. Has an active infection requiring systemic therapy within 7 days prior to the first dose.
  18. Has clinically uncontrolled diabetes mellitus.
  19. Has active tuberculosis, or a history of tuberculosis infection that was not controlled after treatment, or is still receiving anti-tuberculosis therapy; or has active syphilis.
  20. Positive serological virology results: positive for HIV antibody; or positive for HBsAg or HBcAb with HBV-DNA ≥ 500 IU/mL; or positive for HCV antibody with positive HCV-RNA.
  21. Has experienced clinically significant bleeding symptoms or an obvious bleeding tendency within 1 month prior to the first dose.
  22. Has known hypersensitivity or delayed hypersensitivity to certain components or analogues of the IMP in this study.
  23. Has a history of severe neurological or psychiatric disorders, or a history of psychotropic substance abuse or drug abuse, or any other medical condition.
  24. Has known alcohol or drug dependence.
  25. Has insufficient compliance to participate in this clinical study in the investigator's judgment, or the investigator considers that the participant has a history of other serious systemic diseases or other conditions unsuitable for participation in this study.

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: MHB034C for Injection

MHB034C for Injection

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
Phase I Dose Escalation Stage: Incidence of DLT
Tijdsspanne: At the end of Cycle 1 (each cycle is 21 days for Q3W administration and 28 days for Q2W administration)
At the end of Cycle 1 (each cycle is 21 days for Q3W administration and 28 days for Q2W administration)
Phase I Dose Escalation Stage: Incidence of Adverse events (AEs)
Tijdsspanne: from Day1 to 30 days after last dose
from Day1 to 30 days after last dose
Phase I Dose Escalation Stage: Incidence of Serious adverse events (SAEs)
Tijdsspanne: from Day1 to 30 days after last dose
from Day1 to 30 days after last dose
Phase I Dose Escalation Stage: MTD
Tijdsspanne: At the end of Cycle 1 (each cycle is 21 days for Q3W administration and 28 days for Q2W administration)
At the end of Cycle 1 (each cycle is 21 days for Q3W administration and 28 days for Q2W administration)
Phase I Dose Escalation Stage: RP2D
Tijdsspanne: from Day1 to 30 days after last dose
from Day1 to 30 days after last dose
Phase II Dose Expansion Stage: ORR as assessed by the investigator per RECIST v1.1.
Tijdsspanne: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase II Dose Expansion Stage: DCR as assessed by the investigator per RECIST v1.1.
Tijdsspanne: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase II Dose Expansion Stage: DoR as assessed by the investigator per RECIST v1.1.
Tijdsspanne: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase II Dose Expansion Stage: PFS as assessed by the investigator per RECIST v1.1.
Tijdsspanne: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase II Dose Expansion Stage: OS as assessed by the investigator per RECIST v1.1.
Tijdsspanne: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase II Dose Expansion Stage: PFS rates at 6 and 12 months.
Tijdsspanne: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase II Dose Expansion Stage: OS rates at 6 and 12 months.
Tijdsspanne: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group

Secundaire uitkomstmaten

Uitkomstmaat
Tijdsspanne
Phase I Dose Escalation Stage: AUC0-t、AUC0-∞ of MHB034C
Tijdsspanne: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage: Cmax of MHB034C
Tijdsspanne: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage: Tmax of MHB034C
Tijdsspanne: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage: CL of MHB034C
Tijdsspanne: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage: t1/2 of MHB034C
Tijdsspanne: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage: Vss of MHB034C
Tijdsspanne: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage: Ctrough of MHB034C
Tijdsspanne: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage and Phase II Dose Expansion Stage: Positivity rate of anti-MHB034C antibodies (ADA) and their possible neutralizing antibodies (NAb)
Tijdsspanne: through study completion, an average of 2 years
through study completion, an average of 2 years
Phase I Dose Escalation Stage: ORR as assessed by the investigator per RECIST v1.1
Tijdsspanne: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase I Dose Escalation Stage: DCR as assessed by the investigator per RECIST v1.1
Tijdsspanne: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase I Dose Escalation Stage: DoR as assessed by the investigator per RECIST v1.1
Tijdsspanne: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase I Dose Escalation Stage: PFS as assessed by the investigator per RECIST v1.1
Tijdsspanne: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase I Dose Escalation Stage: OS as assessed by the investigator per RECIST v1.1
Tijdsspanne: One year after the last subject was enrolled in the group
One year after the last subject was enrolled in the group
Phase II Dose Expansion Stage: Incidence of AEs
Tijdsspanne: from Day1 to 30 days after last dose
from Day1 to 30 days after last dose
Phase II Dose Expansion Stage: Incidence of SAEs
Tijdsspanne: from Day1 to 30 days after last dose
from Day1 to 30 days after last dose
Phase II Dose Expansion Stage: Concentrations of total antibody, ADC, and free payload in participants after dosing
Tijdsspanne: through study completion, an average of 2 years
through study completion, an average of 2 years

Medewerkers en onderzoekers

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

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 (Geschat)

20 december 2026

Primaire voltooiing (Geschat)

15 juni 2028

Studie voltooiing (Geschat)

19 mei 2029

Studieregistratiedata

Eerst ingediend

29 oktober 2026

Eerst ingediend dat voldeed aan de QC-criteria

4 november 2026

Eerst geplaatst (Werkelijk)

10 november 2026

Updates van studierecords

Laatste update geplaatst (Werkelijk)

10 november 2026

Laatste update ingediend die voldeed aan QC-criteria

4 november 2026

Laatst geverifieerd

1 november 2026

Meer informatie

Termen gerelateerd aan deze studie

Andere studie-ID-nummers

  • MHB034C-A-101

Plan Individuele Deelnemersgegevens (IPD)

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

NEE

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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