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A Study of Lacutoclax (LP-108) in Patients With Relapsed/Refractory CLL/SLL

A Phase 2, Open-Label, Single-Arm, Multicenter Study to Evaluate the Efficacy and Safety of Lacutoclax (LP-108) in Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma

The goal of this clinical trial is to evaluate the efficacy and safety of Lacutoclax, an oral selective BCL-2 inhibitor, in patients with relapsed or refractory chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL). Lacutoclax is a potent and selective BCL-2 inhibitor with relatively weaker inhibitory activity against BCL-XL and BCL-W. Preliminary clinical data have demonstrated promising efficacy and an acceptable safety profile in patients with CLL/SLL and other B-cell non-Hodgkin lymphomas (B-NHLs). This is an open-label, single-arm, multicenter Phase II study evaluating the efficacy and safety of oral Lacutoclax tablets in patients with relapsed or refractory CLL/SLL.

Studieoversikt

Studietype

Intervensjonell

Registrering (Antatt)

75

Fase

  • Fase 2

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

    • Jiangsu
      • Nanjing, Jiangsu, Kina
        • Rekruttering
        • The First Affiliated Hospital of Nanjing Medical University
        • Ta kontakt med:

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:

  1. Patients with confirmed R/R CLL/SLL according to the 2018 International Workshop on Chronic Lymphocytic Leukemia (iwCLL) criteria.
  2. Patients who had previously received standard therapy, experienced disease progression following the most recent line of treatment (excluding intolerance), and had at least one indication for treatment prior to enrollment.
  3. Have at least one measurable lesion.
  4. Age ≥18 years, regardless of sex.
  5. Eastern Cooperative Oncology Group (ECOG) performance status score ≤2.
  6. Life expectancy ≥ 12 weeks.
  7. Adequate coagulation function, liver and kidney function, bone marrow hematopoietic function.
  8. Toxicities from prior anti-tumor therapy have recovered to Grade ≤1 according to NCI CTCAE v5.0.
  9. Male patients and female patients of childbearing potential must agree to use effective contraception during the study and for 90 days after the last dose of Lacutoclax. Female patients of childbearing potential must have a negative pregnancy test before study treatment and must not be breastfeeding. Male patients must not donate sperm during the study and for 90 days after the last dose of Lacutoclax.
  10. Participation is voluntary, requiring signed informed consent and compliance with the treatment regimen and visit schedule.

Exclusion Criteria:

  1. Known hypersensitivity to Lacutoclax or any of its excipients.
  2. Prior treatment with a BCL-2 family inhibitor.
  3. History of or currently suspected Richter's syndrome.
  4. Known or suspected central nervous system (CNS) involvement.
  5. Prior allogeneic hematopoietic stem cell transplantation (allo-HSCT), or autologous hematopoietic stem cell transplantation (auto-HSCT) or chimeric antigen receptor T-cell (CAR-T) therapy within 90 days before the first dose of study treatment.
  6. Received antitumor therapy, investigational agents, major surgery, severe trauma, or live attenuated vaccines within 4 weeks or 5 half-lives prior to the first dose of study treatment.
  7. Received corticosteroids for antitumor purposes, herbal medicines for antitumor treatment, or localized radiotherapy within 14 days prior to the first dose of study treatment.
  8. Use of moderate or strong CYP3A inhibitors within 7 days prior to the first dose of study treatment, or consumption of grapefruit, grapefruit juice, starfruit, or Seville oranges within 3 days prior to dosing.
  9. Prior malignancy other than CLL/SLL within the past 2 years, except for curatively treated basal cell carcinoma, localized squamous cell carcinoma of the skin, carcinoma in situ of the cervix or breast, or other malignancies considered cured.
  10. Major cardiovascular or cerebrovascular events within 6 months prior to the first dose of study treatment.
  11. Presence of any severe and/or uncontrolled systemic disease.
  12. Impaired cardiac function.
  13. Any uncontrolled systemic infection.
  14. Conditions that may impair oral drug administration or significantly affect absorption or pharmacokinetics of the study drug.
  15. Unable to discontinue moderate or strong CYP3A inhibitors or inducers, or sensitive CYP2C8 substrates during the study period.
  16. Primary autoimmune disease requiring immunosuppressive therapy.
  17. Any other condition that, in the investigator's judgment, makes the patient unsuitable for study participation.

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: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Lacutoclax
All participants will receive oral Lacutoclax tablets once daily with dose escalation to a target dose of 400 mg.
Participants will first undergo a dose ramp-up period of at least 4 days (Cycle 0: C0D1-C0D4), followed by continuous administration at the target dose of 400 mg once daily starting from Cycle 1. Each treatment cycle will last 28 days. Treatment will continue until disease progression, unacceptable toxicity, or fulfillment of other criteria for treatment discontinuation.

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
Overall Response Rate (ORR) assessed by Independent Review Committee (IRC)
Tidsramme: Up to approximately 28 months
Up to approximately 28 months

Sekundære resultatmål

Resultatmål
Tidsramme
ORR assessed by Investigator(INV)
Tidsramme: Up to approximately 28 months
Up to approximately 28 months
Complete response(CR) plus complete response with incomplete bone marrow recovery (CRi) rate (CRi applicable only to patients with CLL) assessed by IRC and INV, respectively
Tidsramme: Up to approximately 28 months
Up to approximately 28 months
Time to response (TTR) assessed by IRC and INV, respectively
Tidsramme: Up to approximately 30 months
Up to approximately 30 months
Duration of response (DOR) assessed by IRC and INV, respectively
Tidsramme: Up to approximately 30 months.
Up to approximately 30 months.
Time to first 50% reduction in absolute lymphocyte count (ALC) or normalization of ALC
Tidsramme: Up to approximately 28 months
Up to approximately 28 months
Progression-free survival (PFS) assessed by IRC and INV, respectively
Tidsramme: Up to approximately 30 months
Up to approximately 30 months
Overall Survival
Tidsramme: Up to approximately 30 months
Up to approximately 30 months
Adverse events(AEs) as assessed by CTCAE v5.0
Tidsramme: Up to approximately 30 months
Up to approximately 30 months
Adverse drug reactions (ADRs) related to Lacutoclax
Tidsramme: Up to approximately 30 months
Up to approximately 30 months
Serious adverse events (SAEs)
Tidsramme: Up to approximately 30 months
Up to approximately 30 months
Maximum Plasma Concentration(Cmax)
Tidsramme: From 1 hour prior to administration to 24 hours post-dose
From 1 hour prior to administration to 24 hours post-dose
Time to Maximum Plasma Concentration (Tmax)
Tidsramme: From 1 hour prior to administration to 24 hours post-dose
From 1 hour prior to administration to 24 hours post-dose
Half-life (T1/2)
Tidsramme: From 1 hour prior to administration to 24 hours post-dose
From 1 hour prior to administration to 24 hours post-dose
Area Under the Plasma Concentration-Time Curve from Time Zero to Time t(AUC0-t)
Tidsramme: From 1 hour prior to administration to 24 hours post-dose
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)

14. juli 2026

Primær fullføring (Antatt)

30. mars 2028

Studiet fullført (Antatt)

30. september 2029

Datoer for studieregistrering

Først innsendt

20. mai 2026

Først innsendt som oppfylte QC-kriteriene

20. mai 2026

Først lagt ut (Faktiske)

27. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

30. juli 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

29. juli 2026

Sist bekreftet

1. juli 2026

Mer informasjon

Begreper knyttet til denne studien

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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