- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07570017
A Study of Rocbrutinib Combined With R-GemOx in Patients With Relapsed or Refractory Diffuse Large B-cell Lymphoma
9 september 2026 uppdaterad 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.
Studieöversikt
Status
Rekrytering
Betingelser
Intervention / Behandling
Studietyp
Interventionell
Inskrivning (Beräknad)
42
Fas
- Fas 1
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studiekontakt
- Namn: Qingqing Cai
- Telefonnummer: 086-20-87343355
- E-post: caiqq@sysucc.org.cn
Studera Kontakt Backup
- Namn: Rong Tao
- Telefonnummer: 086-210-64175590
- E-post: hkutao@hotmail.com
Studieorter
-
-
Guangdong
-
Guangzhou, Guangdong, Kina, 510050
- Rekrytering
- Sun Yat-sen University Cancer Center
-
Kontakt:
- Qingqing Cai
- Telefonnummer: 086-20-87343355
- E-post: caiqq@sysucc.org.cn
-
-
Shanghai Municipality
-
Shanghai, Shanghai Municipality, Kina, 200032
- Rekrytering
- Fudan University Shanghai Cancer Center
-
Kontakt:
- Rong Tao
- Telefonnummer: 086-210-64175590
- E-post: hkutao@hotmail.com
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
- Äldre vuxen
Tar emot friska volontärer
Nej
Beskrivning
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
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Icke-randomiserad
- Interventionsmodell: Sekventiell tilldelning
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
|
Experimentell: 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
Andra namn:
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.
|
|
Experimentell: 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
Andra namn:
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.
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
DLTs
Tidsram: 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
Tidsram: 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
Tidsram: From the first administration to 28 days after the last administration
|
From the first administration to 28 days after the last administration
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
ORR
Tidsram: Up to approximately two years
|
Overall Response Rate
|
Up to approximately two years
|
|
TTR
Tidsram: Up to approximately two years
|
Time to Response
|
Up to approximately two years
|
|
DoR
Tidsram: Up to approximately two years
|
Duration of Response
|
Up to approximately two years
|
|
PFS
Tidsram: Up to approximately two years
|
Progression-free Survival
|
Up to approximately two years
|
|
OS
Tidsram: Up to approximately two years
|
Overall Survival
|
Up to approximately two years
|
|
Cmax
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: From 1 hour prior to administration to 24 hours post-dose
|
Half-life
|
From 1 hour prior to administration to 24 hours post-dose
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Faktisk)
25 juni 2026
Primärt slutförande (Beräknad)
31 december 2027
Avslutad studie (Beräknad)
31 juli 2028
Studieregistreringsdatum
Först inskickad
22 april 2026
Först inskickad som uppfyllde QC-kriterierna
29 april 2026
Första postat (Faktisk)
6 maj 2026
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
10 september 2026
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
9 september 2026
Senast verifierad
1 september 2026
Mer information
Termer relaterade till denna studie
Nyckelord
Andra studie-ID-nummer
- LP-168-CN109
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
NEJ
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Nej
Studerar en amerikansk FDA-reglerad produktprodukt
Nej
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