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A Study of Rocbrutinib Combined With R-GemOx in Patients With Relapsed or Refractory Diffuse Large B-cell Lymphoma

A Phase Ib Study to Evaluate the Safety and Efficacy of Rocbrutinib in Combination With Rituximab, Gemcitabine, Oxaliplatin (R-GemOx) in Patients With Refractory or Relapsed Diffuse Large B-cell Lymphoma

This is a multicenter, open-label phase Ib study, evaluating the safety, tolerability, preliminary efficacy and PK characteristics of Rocbrutinib (LP-168) combined with R-GemOx in patients with R/R non-GCB DLBCL. Study includes dose escalation part and dose expansion part. In the dose escalation part, a classic "3+3" design will be used to assess the safety of each specified dose combination. Upon completion of a predefined escalation part, the decision on whether to proceed to the dose expansion part will be based on the safety, PK, and efficacy data of the combination regimen.

Studieoversigt

Status

Ikke rekrutterer endnu

Betingelser

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

42

Fase

  • Fase 1

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Undersøgelse Kontakt Backup

Studiesteder

    • Guangdong
      • Guangzhou, Guangdong, Kina, 510050
        • Sun Yat-sen University Cancer Center
    • Shanghai Municipality
      • Shanghai, Shanghai Municipality, Kina, 200032
        • Fudan University Shanghai Cancer Center

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

Inclusion Criteria:

  • Patients with relapsed or refractory non-GCB DLBCL.
  • Have at least one measurable lesion according to the Lugano Response Criteria 2014.
  • ECOG performance status 0-2 (0-1 for dose escalation part).
  • Life expectancy ≥ 12 weeks.
  • Adequate coagulation function, liver and kidney function, bone marrow hematopoietic function.
  • No plan for autologous/allogeneic hematopoietic stem cell transplantation or chimeric antigen receptor T-cell (CAR-T) therapy.
  • Toxicities from prior anti-tumor therapy have recovered to Grade ≤1 according to NCI CTCAE v5.0.
  • All male subjects and female subjects of childbearing potential must strictly use medically approved contraception throughout the entire study period. All male subjects must also avoid sperm donation during the above period. For women of childbearing potential, the result of serum pregnancy test must be obtained. Women must be non-lactating
  • Subjects must provide adequate tissue and blood samples for exploratory study. Participation is voluntary, requiring signed informed consent and compliance with the treatment regimen and visit schedule.

Exclusion Criteria:

  • Intolerance to Rocbrutinib or any drug in the combination regimen.
  • Prior treatment with a BTK-targeted therapy; prior treatment with R-GemOx.
  • DLBCL transformed from an indolent lymphoma; diagnosis of high-grade or double-hit DLBCL.
  • Chemotherapy, biologic therapy (except CAR-T), immunotherapy or major surgery within 4 weeks of the first dose of study treatment.
  • Small molecule targeted therapy within 4 weeks or within 5 half-lives (whichever is shorter) of the first dose of study treatment.
  • Herbal or proprietary Chinese medicines with antitumor activity or radiotherapy with a limited field of radiation within 7 days of the first dose of study treatment.
  • History of allogeneic hematopoietic stem-cell transplantation (allo-HSCT) or other organ transplantation, or autologous HSCT (auto-HSCT) or chimeric antigen receptor T-cell (CAR-T) therapy within 90 days of the first dose of study treatment.
  • Current corticosteroid therapy at a dose >20 mg/day prednisone equivalent. The prednisone-equivalent dose must have been stable for at least 4 weeks before Cycle 1 Day 1.
  • Unable to discontinue prohibited medications during the study period (strong or moderate CYP3A inhibitors or inducers, P-gp inhibitors, OATP1B3-sensitive substrates, warfarin or other vitamin K antagonists).
  • Known or suspected CNS involvement by lymphoma.
  • Presence of peripheral neuropathy > Grade 1.
  • Any severe and/or uncontrolled systemic disease, or condition affecting drug swallowing or absorption, that in the investigator's judgment makes the subject unsuitable for the study.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Ikke-randomiseret
  • Interventionel model: Sekventiel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Dose Level 1
Patients will receive Rocbrutinib at 150 mg once daily in combination with R-GemOx
Patients will receive Rocbrutinib until disease progression or unacceptable toxicity
Andre navne:
  • LP-168
Patients will receive 6 cycles every 21 days of R-GemOx. Rituximab 375mg/m2 i.v. on day 1 of every cycle. GemOx (gemcitabine 1000mg/m2 plus oxaliplatin 100mg/m2) i.v. on day 2 of each cycle.
Eksperimentel: Dose Level 2
Patients will receive Rocbrutinib at 200 mg once daily in combination with R-GemOx
Patients will receive Rocbrutinib until disease progression or unacceptable toxicity
Andre navne:
  • LP-168
Patients will receive 6 cycles every 21 days of R-GemOx. Rituximab 375mg/m2 i.v. on day 1 of every cycle. GemOx (gemcitabine 1000mg/m2 plus oxaliplatin 100mg/m2) i.v. on day 2 of each cycle.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
DLTs
Tidsramme: At the end of Cycle 1 (the length of cycle 1 is 21 days)
Dose-Limiting Toxicities
At the end of Cycle 1 (the length of cycle 1 is 21 days)
MTD
Tidsramme: At the end of Cycle 1 (the length of cycle 1 is 21 days)
Maximum Tolerated Dose
At the end of Cycle 1 (the length of cycle 1 is 21 days)
Adverse events as assessed by CTCAE v5.0
Tidsramme: From the first administration to 28 days after the last administration
From the first administration to 28 days after the last administration

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
ORR
Tidsramme: Up to approximately two years
Overall Response Rate
Up to approximately two years
TTR
Tidsramme: Up to approximately two years
Time to Response
Up to approximately two years
DoR
Tidsramme: Up to approximately two years
Duration of Response
Up to approximately two years
PFS
Tidsramme: Up to approximately two years
Progression-free Survival
Up to approximately two years
OS
Tidsramme: Up to approximately two years
Overall Survival
Up to approximately two years
Cmax
Tidsramme: From 1 hour prior to administration to 24 hours post-dose
Maximum Plasma Concentration
From 1 hour prior to administration to 24 hours post-dose
Tmax
Tidsramme: From 1 hour prior to administration to 24 hours post-dose
Time to Maximum Plasma Concentration
From 1 hour prior to administration to 24 hours post-dose
AUC0-t
Tidsramme: From 1 hour prior to administration to 24 hours post-dose
Area Under the Plasma Concentration-Time Curve from Time Zero to Time t
From 1 hour prior to administration to 24 hours post-dose
t1/2
Tidsramme: From 1 hour prior to administration to 24 hours post-dose
Half-life
From 1 hour prior to administration to 24 hours post-dose

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

30. maj 2026

Primær færdiggørelse (Anslået)

31. december 2027

Studieafslutning (Anslået)

31. juli 2028

Datoer for studieregistrering

Først indsendt

22. april 2026

Først indsendt, der opfyldte QC-kriterier

29. april 2026

Først opslået (Faktiske)

6. maj 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

6. maj 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

29. april 2026

Sidst verificeret

1. april 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • LP-168-CN109

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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Kliniske forsøg med DLBCL

Kliniske forsøg med Rocbrutinib

Abonner