- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07591168
A Study of BL-M11D1 in Patients With Relapsed/Refractory Myelodysplastic Syndromes
9. maj 2026 opdateret af: Sichuan Baili Pharmaceutical Co., Ltd.
A Phase Ib/II Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic Characteristics, and Preliminary Efficacy of BL-M11D1 for Injection in Patients With Relapsed/Refractory Myelodysplastic Syndromes
This study is an open-label, multicenter, non-randomized Phase Ib/II clinical study to evaluate the safety, tolerability, and pharmacokinetic characteristics of BL-M11D1 for injection in patients with relapsed/refractory myelodysplastic syndromes.
Studieoversigt
Status
Ikke rekrutterer endnu
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
The study consists of two phases: a dose-exploration phase (Phase Ib) and a dose-expansion phase (Phase II).
Undersøgelsestype
Interventionel
Tilmelding (Anslået)
92
Fase
- Fase 2
- Fase 1
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Sa Xiao, PHD
- Telefonnummer: 15013238943
- E-mail: xiaosa@baili-pharm.com
Studiesteder
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-
Tianjin Municipality
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Tianjin, Tianjin Municipality, Kina
- Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Sciences
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Kontakt:
- Zhijian Xiao
- Telefonnummer: 022-23909083
- E-mail: zjxiao@ihcams.ac.cn
-
-
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:
- Voluntarily sign the informed consent form and comply with the protocol requirements;
- No gender restrictions;
- Age: ≥18 years and ≤75 years;
- Expected survival time ≥3 months;
- Relapsed/refractory CD33+ MDS;
- Morphological assessment showing blasts in bone marrow ≥5% and <20%;
- Eastern Cooperative Oncology Group (ECOG) performance status ≤2;
- Toxicities from prior anti-tumor therapy must have recovered to ≤ Grade 1 as defined by NCI-CTCAE v6.0;
- Meet the required organ function levels;
- For premenopausal women of childbearing potential, a pregnancy test (serum/urine) must be negative within 7 days before starting treatment, and they must not be breastfeeding; all enrolled trial participants (regardless of gender) must practice adequate barrier contraception throughout the entire treatment period and for 6 months after treatment completion.
Exclusion Criteria:
- Use of chemotherapy, biotherapy, immunotherapy, etc., within 4 weeks or 5 half-lives prior to the first dose;
- Presence of uncorrected folate deficiency or vitamin B12 deficiency, etc.;
- History of severe cardiovascular or cerebrovascular disease;
- Thromboembolic events requiring therapeutic intervention within 6 months prior to screening;
- Active autoimmune diseases and inflammatory diseases;
- History of extensive bowel resection or presence of Crohn's disease, ulcerative colitis, chronic diarrhea, or intestinal obstruction;
- Diagnosis of another malignancy within 5 years prior to the first dose;
- Poorly controlled hypertension;
- Poorly controlled hyperglycemia or diabetes mellitus;
- Pulmonary diseases classified as Grade ≥3 according to CTCAE v6.0, etc.;
- Trial participants with central nervous system involvement;
- Trial participants with extramedullary involvement;
- Trial participants with a history of allergy to recombinant humanized antibodies or chimeric human-mouse antibodies, or hypersensitivity to any excipient component of BL-M11D1;
- Prior organ transplantation or hematopoietic stem cell transplantation;
- Positive for human immunodeficiency virus antibody, active tuberculosis, active hepatitis B virus infection, or active hepatitis C virus infection;
- Active fungal, bacterial, or viral infections;
- History of severe neurological or psychiatric disorders;
- Trial participants with clinically significant bleeding or obvious bleeding tendency within 4 weeks prior to signing informed consent;
- Presence of clinically symptomatic pleural, peritoneal, or pericardial effusion requiring repeated drainage;
- Participation in another clinical trial within 4 weeks or 5 half-lives prior to the first dose;
- Pregnant or breastfeeding women;
- Other conditions deemed by the investigator to make the participant unsuitable for participation in this clinical trial.
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: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Eksperimentel: BL-M11D1
Participants receive BL-M11D1 for the first cycle (4 weeks).
Participants with clinical benefit could receive additional treatment for more cycles.
The administration will be terminated because of disease progression or intolerable toxicity occurring or other reasons.
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Administration ved intravenøs infusion i en cyklus på 4 uger.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Fase II: Objektiv responsrate (ORR)
Tidsramme: Op til cirka 24 måneder
|
ORR er defineret som procentdelen af deltagere, der har en CR (forsvinden af alle mållæsioner) eller PR (mindst et 30 % fald i summen af diametre af mållæsioner).
Procentdelen af deltagere, der oplever en bekræftet CR eller PR, er i henhold til RECIST 1.1.
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Op til cirka 24 måneder
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Phase Ib: Recommended Phase II Dose (RP2D)
Tidsramme: Up to approximately 24 months
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The RP2D is defined as the dose level chosen by the sponsor (in consultation with the investigators) for phase II study, based on safety, tolerability, efficacy, PK, and PD data collected during the dose escalation study of BL-M11D1.
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Up to approximately 24 months
|
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Phase Ib: Treatment-Emergent Adverse Event (TEAE)
Tidsramme: Up to approximately 24 months
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TEAE is defined as any unfavorable and unintended change in the structure, function, or chemistry of the body temporally emerging, or any worsening (i.e., any clinically significant adverse change in frequency and/or intensity) of a pre-existing condition during the treatment of BL-M11D1.
The type, frequency and severity of TEAE will be evaluated during the treatment of BL-M11D1.
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Up to approximately 24 months
|
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Phase II: Complete Response (CR)
Tidsramme: Up to approximately 24 months
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Complete Response (CR) is defined as the disappearance of all target lesions, with any pathological lymph nodes (whether target or non-target) having a short axis diameter reduced to <10 mm.
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Up to approximately 24 months
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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AUC0-t
Tidsramme: Op til cirka 24 måneder
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AUC0-t er defineret som areal under serumkoncentration-tid-kurven fra tidspunkt 0 til tidspunktet for den sidste målelige koncentration.
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Op til cirka 24 måneder
|
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Cmax
Tidsramme: Op til cirka 24 måneder
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Den maksimale serumkoncentration (Cmax) af BL-M11D1 vil blive undersøgt.
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Op til cirka 24 måneder
|
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Tmax
Tidsramme: Op til cirka 24 måneder
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Tid til maksimal serumkoncentration (Tmax) af BL-M11D1 vil blive undersøgt.
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Op til cirka 24 måneder
|
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Ctrough
Tidsramme: Op til cirka 24 måneder
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Ctrough er defineret som den laveste serumkoncentration af BL-M11D1 før den næste dosis gives.
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Op til cirka 24 måneder
|
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ADA (anti-drug antibody)
Tidsramme: Op til ca. 24 måneder
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Hyppigheden af anti-BL-M11D1-antistof (ADA) vil blive undersøgt.
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Op til ca. 24 måneder
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T1/2
Tidsramme: Up to approximately 24 months
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Half-life (T1/2) of BL-M11D1 will be investigated.
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Up to approximately 24 months
|
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CL (Clearance)
Tidsramme: Up to approximately 24 months
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CL in the serum of BL-M11D1 per unit of time will be investigated.
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Up to approximately 24 months
|
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Phase II: Duration of Response (DOR)
Tidsramme: Up to approximately 24 months
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The DOR for a responder is defined as the time from the participant's initial objective response to the first date of either disease progression or death, whichever occurs first.
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Up to approximately 24 months
|
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Phase II: Hematologic Improvement (HI)
Tidsramme: Up to approximately 24 months
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HI is defined as achieving a predefined threshold of improvement in the erythroid, platelet, or neutrophil lineages according to the IWG 2006 and IWG 2023 criteria, with a duration of no less than 8 weeks.
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Up to approximately 24 months
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Phase II: AML Transformation Rate
Tidsramme: Up to approximately 24 months
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The AML transformation rate is defined as the first confirmed event of transformation to acute myeloid leukemia according to WHO criteria (bone marrow blasts ≥20% or presence of extramedullary infiltration).
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Up to approximately 24 months
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Samarbejdspartnere
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)
1. maj 2026
Primær færdiggørelse (Anslået)
1. december 2028
Studieafslutning (Anslået)
1. december 2028
Datoer for studieregistrering
Først indsendt
9. maj 2026
Først indsendt, der opfyldte QC-kriterier
9. maj 2026
Først opslået (Faktiske)
15. maj 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
15. maj 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
9. maj 2026
Sidst verificeret
1. maj 2026
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- BL-M11D1-102
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
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Neuren Pharmaceuticals LimitedRekrutteringPhelan-McDermid syndromForenede Stater
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University of California, DavisNational Cancer Institute (NCI); Celgene; Pharmacyclics LLC.AfsluttetTidligere behandlet myelodysplastisk syndrom | Myelodysplastisk syndrom | Terapi-relateret myelodysplastisk syndrom | Sekundært myelodysplastisk syndrom | Refraktært højrisiko myelodysplastisk syndromForenede Stater
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Riphah International UniversityAfsluttet
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Shaare Zedek Medical CenterUkendtPræmenstruelt syndrom - PMS
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Kliniske forsøg med BL-M11D1
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Sichuan Baili Pharmaceutical Co., Ltd.RekrutteringRecidiverende/refraktær akut myeloid leukæmi (R/R AML)Kina
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SystImmune Inc.RekrutteringRecidiverende/Refraktær Akut Myeloid LeukæmiForenede Stater
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Sichuan Baili Pharmaceutical Co., Ltd.Baili-Bio (Chengdu) Pharmaceutical Co., Ltd.Ikke rekrutterer endnu
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Sichuan Baili Pharmaceutical Co., Ltd.Baili-Bio (Chengdu) Pharmaceutical Co., Ltd.RekrutteringTilbagefaldende eller refraktære lymfoide maligniteterKina
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Sichuan Baili Pharmaceutical Co., Ltd.Baili-Bio (Chengdu) Pharmaceutical Co., Ltd.Rekruttering
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Sichuan Baili Pharmaceutical Co., Ltd.SystImmune Inc.; Baili-Bio (Chengdu) Pharmaceutical Co., Ltd.RekrutteringBrystkræft | Lokalt avanceret eller metastatisk solid tumorKina
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Sichuan Baili Pharmaceutical Co., Ltd.SystImmune Inc.; Baili-Bio (Chengdu) Pharmaceutical Co., Ltd.Aktiv, ikke rekrutterende
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Sichuan Baili Pharmaceutical Co., Ltd.SystImmune Inc.; Baili-Bio (Chengdu) Pharmaceutical Co., Ltd.Aktiv, ikke rekrutterendeSolid tumor | Lokalt avancerede eller metastatiske tumorer i fordøjelseskanalenKina
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Sichuan Baili Pharmaceutical Co., Ltd.Baili-Bio (Chengdu) Pharmaceutical Co., Ltd.RekrutteringFaste tumorer | Gastrointestinale tumorerKina
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Sichuan Baili Pharmaceutical Co., Ltd.Baili-Bio (Chengdu) Pharmaceutical Co., Ltd.RekrutteringSolid tumor | Ikke småcellet lungekræftKina