- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT07570017
A Study of Rocbrutinib Combined With R-GemOx in Patients With Relapsed or Refractory Diffuse Large B-cell Lymphoma
9. september 2026 oppdatert av: Guangzhou Lupeng Pharmaceutical Company LTD.
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.
Studieoversikt
Status
Rekruttering
Forhold
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Antatt)
42
Fase
- Fase 1
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiekontakt
- Navn: Qingqing Cai
- Telefonnummer: 086-20-87343355
- E-post: caiqq@sysucc.org.cn
Studer Kontakt Backup
- Navn: Rong Tao
- Telefonnummer: 086-210-64175590
- E-post: hkutao@hotmail.com
Studiesteder
-
-
Guangdong
-
Guangzhou, Guangdong, Kina, 510050
- Rekruttering
- Sun Yat-sen University Cancer Center
-
Ta kontakt med:
- Qingqing Cai
- Telefonnummer: 086-20-87343355
- E-post: caiqq@sysucc.org.cn
-
-
Shanghai Municipality
-
Shanghai, Shanghai Municipality, Kina, 200032
- Rekruttering
- Fudan University Shanghai Cancer Center
-
Ta kontakt med:
- Rong Tao
- Telefonnummer: 086-210-64175590
- E-post: hkutao@hotmail.com
-
-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Voksen
- Eldre voksen
Tar imot friske frivillige
Nei
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
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Ikke-randomisert
- Intervensjonsmodell: Sekvensiell tildeling
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Eksperimentell: 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 navn:
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.
|
|
Eksperimentell: 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 navn:
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.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
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 |
Tiltaksbeskrivelse |
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
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Faktiske)
25. juni 2026
Primær fullføring (Antatt)
31. desember 2027
Studiet fullført (Antatt)
31. juli 2028
Datoer for studieregistrering
Først innsendt
22. april 2026
Først innsendt som oppfylte QC-kriteriene
29. april 2026
Først lagt ut (Faktiske)
6. mai 2026
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
10. september 2026
Siste oppdatering sendt inn som oppfylte QC-kriteriene
9. september 2026
Sist bekreftet
1. september 2026
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Andre studie-ID-numre
- LP-168-CN109
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
NEI
Legemiddel- og utstyrsinformasjon, studiedokumenter
Studerer et amerikansk FDA-regulert medikamentprodukt
Nei
Studerer et amerikansk FDA-regulert enhetsprodukt
Nei
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