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A Study of DXC006 With Immune Checkpoint Inhibitors or Platinum for Small Cell Lung Cancer.

27. Mai 2026 aktualisiert von: Hangzhou DAC Biotechnology Co., Ltd.

A Phase Ib/II Study to Evaluate the Safety and Efficacy of DXC006 for Injection Combined With Immune Checkpoint Inhibitors or Platinum-Based Agents in Patients With Small Cell Lung Cancer.

This is a Phase Ib/II, open-label clinical study designed to evaluate the safety, tolerability, preliminary anti-tumor activity, recommended Phase 2 dose (RP2D), pharmacokinetic (PK) characteristics, and immunogenicity of DXC006 in combination with an immune checkpoint inhibitor (ICI) or platinum-based chemotherapy in patients with small cell lung cancer (SCLC).

Studienübersicht

Studientyp

Interventionell

Einschreibung (Geschätzt)

200

Phase

  • Phase 2
  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studienorte

    • Guangdong
      • Guangzhou, Guangdong, China, 510060
        • Sun Yat-sen University Cancer Center
        • Kontakt:

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

Inclusion Criteria:

  1. Voluntarily signed informed consent and willingness to comply with the protocol requirements.
  2. Male or female.
  3. Age ≥18 years and ≤75 years.
  4. Life expectancy ≥3 months.
  5. Eastern Cooperative Oncology Group (ECOG) performance status score of 0-2.
  6. Histologically or cytologically confirmed small cell lung cancer (SCLC).
  7. Toxicity from prior anti-tumor therapy has resolved to ≤ Grade 1 as defined by NCI-CTCAE version 6.0 (except alopecia); peripheral neuropathy must have completely resolved.
  8. Adequate hepatic, renal, coagulation, and cardiac function.
  9. The participant and their spouse agree to use effective barrier or pharmacologic contraception (excluding rhythm method) from the time of signing the informed consent until 6 months after the last dose of study treatment.

Exclusion Criteria:

  1. Histologically or cytologically confirmed combined SCLC, NSCLC, sarcomatoid carcinoma, or large cell neuroendocrine carcinoma.
  2. Within 14 days prior to the first dose: underwent plasmapheresis; received systemic corticosteroid therapy at a daily dose >10 mg prednisone or equivalent (or equivalent anti-inflammatory activity) for more than 3 consecutive days (short-term use for prevention of contrast media allergy is permitted).
  3. Prior allogeneic hematopoietic stem cell transplantation (HSCT) or history of solid organ transplantation.
  4. Prior treatment with CD56-targeted therapy.
  5. Symptomatic brain metastases or leptomeningeal metastases.
  6. History of severe or life-threatening immune-related adverse events or infusion-related reactions (including permanent discontinuation of immuno-oncology therapy due to intolerance).
  7. Active autoimmune disease or immunodeficiency, or a history of such conditions.
  8. Evidence of significant cardiovascular risk.
  9. Dyspnea or current requirement for continuous supplemental oxygen therapy, or current active pneumonitis or interstitial lung disease (except mild cases as determined by the investigator).
  10. History of other primary malignancies, with the exception of malignancies that have been cured and have a very low risk of recurrence within 5 years, such as basal cell carcinoma or squamous cell carcinoma of the skin, or carcinoma in situ of the cervix or breast.
  11. Severe non-healing wound, ulcer, or bone fracture; or major surgery within 28 days prior to dosing, or anticipated major surgery during the study period.
  12. History of hypersensitivity to any component or excipient of DXC006, immune checkpoint inhibitors, or platinum-based chemotherapy.
  13. Active hepatitis B (HBV-DNA above the upper limit of normal at the central laboratory or >1000 copies/mL); hepatitis C infection (positive hepatitis C antibody or positive HCV RNA PCR result).
  14. Known positive serology for human immunodeficiency virus (HIV); active syphilis (patients with positive syphilis antibody only are eligible); potential active pulmonary tuberculosis (chest imaging within 3 months prior to the first dose suggestive of active tuberculosis infection).
  15. Active bleeding within 30 days prior to screening, or risk of major gastrointestinal bleeding or hemoptysis as determined by the investigator; or hereditary bleeding tendency, coagulopathy, or bleeding symptoms requiring other medical intervention.
  16. Severe arterial or venous thromboembolic events within 6 months prior to study drug administration, such as cerebrovascular accident (including transient ischemic attack), deep vein thrombosis, or pulmonary embolism.
  17. Positive serum pregnancy test or currently breastfeeding female participants.
  18. Active infection requiring medical therapy (CTCAE Grade ≥2); uncontrollable pleural effusion, ascites, or pericardial effusion requiring repeated drainage.
  19. Administration of live attenuated vaccines within 28 days prior to the first dose.
  20. Other conditions that, in the judgment of the investigator, may affect the patient's participation in the study.
  21. Poor general condition, such as requirement for mechanical ventilation and/or intravenous catecholamine infusion, and/or severe neurological impairment, coma, and/or quadriplegia with complete loss of communication ability (deafness, blindness, aphasia); uncontrolled seizures; other psychiatric disorders that may affect study participation.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Nicht randomisiert
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: DXC006 + ICI
Participants receive DXC006 intravenously on Day 1 every 3 weeks.
Participants receive Toripalimab intravenously on Day 1 every 3 weeks.
Experimental: DXC006 + Platinum(Carboplatin )
Participants receive DXC006 intravenously on Day 1 every 3 weeks.
Participants receive Carboplatin intravenously on Day 1 every 3 weeks (up to 6 cycles).
Experimental: DXC006 + Platinum(Cisplatin )
Participants receive DXC006 intravenously on Day 1 every 3 weeks.
Participants receive Cisplatin intravenously on Day 1 every 3 weeks (up to 6 cycles).

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
Progression Free Survival (PFS)
Zeitfenster: From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 year.
From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 year.
6-month progression-free survival rate
Zeitfenster: From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 6 months.
From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 6 months.
Recommended Phase 2 Dose (RP2D)
Zeitfenster: Final RP2D confirmation upon completion of the Phase Ib (up to 12 months).
Final RP2D confirmation upon completion of the Phase Ib (up to 12 months).
Measurement of objective response rate (ORR) per RECIST 1.1
Zeitfenster: From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 year.
From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 year.
Measurement of disease control rate (DCR)
Zeitfenster: From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 year.
From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 year.
Incidence of Adverse Events (AEs)
Zeitfenster: After first infusion of study drug, through study completion an average of 2 year.
After first infusion of study drug, through study completion an average of 2 year.

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
Maximum observed serum or plasma concentration (Cmax)
Zeitfenster: Through study completion an average of 1 year.
Through study completion an average of 1 year.
Maximum serum drug time(Tmax)
Zeitfenster: Through study completion an average of 1 year.
Through study completion an average of 1 year.
Apparent volume of distribution(Vd)
Zeitfenster: Through study completion an average of 1 year.
Through study completion an average of 1 year.
Volume of distribution at steady state (Vss)
Zeitfenster: Through study completion an average of 1 year.
Through study completion an average of 1 year.
Terminal phase elimination half life (t½)
Zeitfenster: Through study completion an average of 1 year.
Through study completion an average of 1 year.
Area under the serum or plasma concentration time curve from 0 to the last measurable point (AUC0-t).
Zeitfenster: Through study completion an average of 1 year.
Through study completion an average of 1 year.
Area under the serum or plasma concentration time curve from 0 to infinity (AUC0-inf)
Zeitfenster: Through study completion an average of 1 year.
Through study completion an average of 1 year.
Clearance (CL)
Zeitfenster: Through study completion an average of 1 year.
Through study completion an average of 1 year.
Ctrough
Zeitfenster: Through study completion an average of 1 year.
Through study completion an average of 1 year.
Anti-drug antibodies (ADA)
Zeitfenster: Through study completion an average of 1 year.
Through study completion an average of 1 year.
Overall Survival (OS)
Zeitfenster: From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 year.
From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 year.
Duration of response (DOR)
Zeitfenster: From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 year.
From date of enrollment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 2 year.

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. Juni 2026

Primärer Abschluss (Geschätzt)

1. Juni 2028

Studienabschluss (Geschätzt)

30. Dezember 2030

Studienanmeldedaten

Zuerst eingereicht

24. April 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

24. April 2026

Zuerst gepostet (Tatsächlich)

30. April 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

29. Mai 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

27. Mai 2026

Zuletzt verifiziert

1. März 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

NEIN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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