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Study of PM54 in Combination With Immunotherapy in Adult Participants With Advanced Malignancies

keskiviikko 29. heinäkuuta 2026 päivittänyt: PharmaMar

A Multicenter, Open-label, Phase 1/2 Safety Run-in and Expansion Study of PM54 in Combination With Immunotherapy Evaluating Safety and Efficacy in Adult Participants Who Were Previously Treated for Advanced Malignancies

The main purpose of the study is to evaluate the safety, tolerability and recommended dose of PM54 in combination with pembrolizumab. To assess the antitumor activity of PM54 in combination with pembrolizumab in terms of clinical benefit rate (CBR) and objective response rate (ORR) based on investigator's assessment in participants in other cohorts.

Tutkimuksen yleiskatsaus

Opintotyyppi

Interventio

Ilmoittautuminen (Arvioitu)

119

Vaihe

  • Vaihe 2
  • Vaihe 1

Yhteystiedot ja paikat

Tässä osiossa on tutkimuksen suorittajien yhteystiedot ja tiedot siitä, missä tämä tutkimus suoritetaan.

Opiskeluyhteys

Opiskelupaikat

      • Barcelona, Espanja
        • Ei vielä rekrytointia
        • Institut Catala D'oncologia
      • Madrid, Espanja
        • Rekrytointi
        • Hospital General Universitario Gregorio Marañón
      • Madrid, Espanja
        • Rekrytointi
        • Clinica Universidad de Navarra (Cun)
      • Madrid, Espanja
        • Rekrytointi
        • START Madrid - Hospital Universitario Fundacion Jimenez D
      • Pamplona, Espanja
        • Rekrytointi
        • Clinica Universidad de Navarra (Cun)
    • New York
      • New York, New York, Yhdysvallat, 11042
        • Rekrytointi
        • START New York
    • Texas
      • Fort Worth, Texas, Yhdysvallat, 76104
        • Rekrytointi
        • START Dallas
      • Houston, Texas, Yhdysvallat, 77030
        • Rekrytointi
        • The University of Texas MD Anderson Cancer Center
      • Houston, Texas, Yhdysvallat, 77054
        • Rekrytointi
        • NEXT Houston
      • Irving, Texas, Yhdysvallat, 75039
        • Rekrytointi
        • NEXT Dallas
    • Virginia
      • Fairfax, Virginia, Yhdysvallat, 22031
        • Rekrytointi
        • NEXT Virginia

Osallistumiskriteerit

Tutkijat etsivät ihmisiä, jotka sopivat tiettyyn kuvaukseen, jota kutsutaan kelpoisuuskriteereiksi. Joitakin esimerkkejä näistä kriteereistä ovat henkilön yleinen terveydentila tai aiemmat hoidot.

Kelpoisuusvaatimukset

Opintokelpoiset iät

  • Aikuinen
  • Vanhempi Aikuinen

Hyväksyy terveitä vapaaehtoisia

Ei

Kuvaus

Inclusion Criteria:

  1. Voluntarily signed and dated written informed consent, obtained before the start of any study-specific procedures.
  2. Adults (greater than or equal to [>=]18 years or legal consenting age, per local regulations), and able to provide free and informed consent for study participation.
  3. Have a pathologically confirmed diagnosis of advanced malignancy.
  4. Have advanced disease, as defined by progressive, relapsed, or metastatic disease that is not amenable to multimodal ablative or excisional treatments with curative intent, according to international guidelines.
  5. Have measurable disease according to RECIST1.1 (or mRECIST v1.1 where applicable).
  6. Have experienced objective disease progression on or following the prior line(s) of systemic therapy, as determined either by (1) RECIST v1.1 or equivalent, or (2) by investigator's assessment of clinical progression of disease together with objective evidence of increased tumor burden even if not meeting criteria for progressive disease per RECIST v1.1 or equivalent.
  7. Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) of 0 or 1 at screening.
  8. Individuals with central nervous system (CNS) metastases are eligible, as long as all of the following are met:

    1. Asymptomatic or minimally symptomatic and stable, with no worsening symptoms in the 4 weeks prior to start of study intervention.
    2. Does not require systemic corticosteroids in excess of an equivalent prednisone dose of 5 milligrams per day (mg/day).
    3. Has undergone surgery or radiation and recovered of the effects thereof or are undergoing active surveillance for small-volume CNS metastases with no immediate risk of worsening. A minimum of 2 weeks must have elapsed between the end of whole-brain radiation treatment and study intervention.
    4. Have not had an epileptic seizure within the 4 weeks prior to start of anticancer treatment and are either free of antiepileptics or on a stable dose prescribed as prophylaxis.
  9. Adequate laboratory parameters, as specified below, within 7 days of start of study intervention:

    1. Absolute neutrophil count (ANC) >=1.5*10^9 per liter, platelet count >=100*10^9 per liter, and hemoglobin >=9 gram per deciliter (g/dL).
    2. Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) less than or equal to [<=] 3.0*the upper limit of normal (ULN).
    3. Total bilirubin <=1.0*ULN; up to 1.5*ULN for participants with Gilbert's syndrome.
    4. Creatinine clearance >=30 milliliter per minute (mL/min), calculated using the Cockcroft and Gault's formula.
    5. Serum albumin >=3 g/dL. Albumin infusion to increase the blood level in order to fulfill this inclusion criterion is strictly forbidden.
    6. Creatine kinase <=2.5*ULN.
  10. Recovered from the effects of any prior surgery or radiation.
  11. No ongoing toxicities from prior anticancer treatment of Grade >1 (per National Cancer Institute (NCI)-Common Terminology Criteria for Adverse Events (CTCAE) verison6.0), except for alopecia and other Grade 2 toxicities that are considered by the investigator to have stabilized/resolved with sequelae and are not at risk of worsening with study intervention. Residual Grade 1 to 2 toxicities from prior immunotherapy -which may include hypo- or hyperthyroidism, type 1 diabetes, hyperglycemia, and adrenal insufficiency - are allowed, if stable and on a stable dose of replacement therapy as applicable.
  12. Is willing to undergo trial procedures as specified in the protocol, including provision of biologic samples, as well as any study restrictions.
  13. Evidence of non-childbearing status for women of childbearing potential (WOCBP). WOCBP must agree to use a highly effective contraceptive measure during the course of the trial and up to 7 months after the last study intervention infusion. Fertile male participants with WOCBP partners should use condoms during treatment and for 4 months following the last study intervention infusion.

Exclusion Criteria:

  1. Prior treatment with PM54 or any other ecteinascidin agent, including ecubectedin, trabectedin, and lurbinectedin.
  2. History of hypersensitivity to PM54, pembrolizumab, or any of the inactive ingredients.
  3. History of other malignancies within 3 years prior to start of study intervention, except adequately resected non-melanoma skin cancer or other in-situ disease at neglectable risk of relapse.
  4. Presence of carcinomatous meningitis.
  5. Presence of any of these medical conditions

    Cardiovascular:

    1. History of myocardial, CNS, or other arterial infarction within 6 months before the start of study intervention.
    2. Heart failure Class II or higher according to the New York Heart Association or left ventricular ejection fraction <45 percent (%) per echocardiogram or multigated acquisition scan.
    3. Symptomatic arrhythmia or other significant electrocardiogram (ECG) abnormalities that in the opinion of the investigator pose an increased risk of complications.
    4. Corrected QT interval (QTc) >470 milliseconds (ms) on the screening ECG or history of a long QT syndrome.

      Respiratory

    5. History of interstitial lung disease (ILD) or pneumonitis that have required steroids or other forms of immunosuppression, or any ongoing or suspicion of ILD.
    6. Severe underlying lung disorder, as per investigator's assessment that can include but not restricted to chronic obstructive pulmonary disease, asthma, restrictive lung disease, or significant pleural effusions not related to the study condition.
    7. New onset or worsening of pulmonary embolism or deep vein thrombosis within the previous 2 months, or any history thereof if no stable dose of anticoagulant regimen has been achieved.

      Other

    8. History of autoimmune or connective tissue disease that (a) in the opinion of the investigator may have a significant risk of worsening with study intervention or (b) has a history or risk of significant mg/day of prednisone equivalent or other systemic immunosuppressants in the previous 1 year to control a disease flare.
    9. Uncontrolled infection requiring antimicrobial agents or unexplained fever within 3 days of the first scheduled day of dosing. Participants with tumor fever may be enrolled if infectious etiology has been adequately ruled out. j. Prior bone marrow or stem cell transplantation.
  6. Has any other medical, behavioral, or social condition that, in the opinion of the investigator, makes the participant ineligible to receive PM54, pembrolizumab, or undergo key trial procedures.
  7. Exposure to the anticancer products/treatments below, without adequate washout period prior to first dose of study intervention. Note that hormonal therapy received for the adjuvant treatment of tumors at a low risk of relapse is allowed.

    Products/treatments and washout periods:

    1. Traditional Chinese or herbal medicine with the intent to treat cancer or with known effects on drug metabolism: 28 days.
    2. Live, attenuated vaccines: 30 days.
    3. Chemotherapy: 21 days.
    4. Antibodies and antidrug conjugates: 28 days.
    5. Targeted agents and small molecules: 2 weeks or 5 half-lives, whichever is longer.
    6. Major surgery: 4 weeks. Note: Surgeries typically performed in an outpatient setting are not considered major, even if light sedation or an inpatient stay for oversight was needed.
    7. Whole-brain radiation therapy, stereotactic therapy, palliative radiation for symptom control and minor impact on bone marrow: 2 weeks.
    8. Other radiation therapy: 4 weeks.
    9. Any medication associated with increased risk of torsade de pointes, except if considered indicated by the investigator, ideally for short duration, under medical monitoring and if no other risk factors for torsade de pointes are present such as prolonged QTc or significant electrolyte abnormalities.: 5 half-lives.
    10. Strong or moderate inhibitors or inducers of cytochrome (CYP) 3A4: 2 weeks.
    11. Corticosteroids: must be <= 10 mg/day of prednisone equivalent within 3 days of start of study intervention. The investigator is encouraged to review indication for ongoing use of corticosteroids and consider de-escalation or interruption if appropriate.
  8. Active HIV infection. Inclusion is allowed if:

    1. Undergoing adequate anti-viral treatment and regular clinical oversight with good compliance.
    2. Undetectable human immunodeficiency virus (HIV) viral load.
    3. CD4+ lymphocyte count over 350 per millimeter cube.
    4. No evidence or suspicion of opportunistic infection. Note: The investigator should obtain and provide the sponsor with written documentation of the above, assessed by a medical doctor experienced in the management of individuals with HIV.
  9. Individuals with detectable hepatitis C virus (HCV) ribonucleic acid (RNA), which should be tested in case of positive anti-HCV antibody test.
  10. Positive serology test of hepatitis B surface antigen (HBsAg) with hepatitis B virus (HBV) DNA >= 1000 International Units per milliliter (IU/mL). Hepatitis B virus (HBV) DNA test is mandatory in case of HBsAg+. Individuals with detectable HBV DNA <1000 IU/mL or suspected occult HBV infection must undergo prophylaxis of HBV reactivation in order to be eligible.
  11. Individuals with a short-term risk of anatomic complications from involvement of critical structures such as major vessels, large airways, and vertebral spine.
  12. Women who are pregnant or breastfeeding and fertile participants (men and women) who are not using a highly effective method of contraception (see inclusion criterion No. 13).

Opintosuunnitelma

Tässä osiossa on tietoja tutkimussuunnitelmasta, mukaan lukien kuinka tutkimus on suunniteltu ja mitä tutkimuksella mitataan.

Miten tutkimus on suunniteltu?

Suunnittelun yksityiskohdat

  • Ensisijainen käyttötarkoitus: Hoito
  • Jako: Ei satunnaistettu
  • Inventiomalli: Peräkkäinen tehtävä
  • Naamiointi: Ei mitään (avoin tarra)

Aseet ja interventiot

Osallistujaryhmä / Arm
Interventio / Hoito
Kokeellinen: Part 1 (safety Run-in): PM54 + Pembrolizumab
Participants will initially receive a low dose of PM54. If the low dose level is tolerated, PM54 will be escalated to the high dose level in combination with pembrolizumab until a suitable dose of PM54 is established or until clinical or objective disease progression, withdrawal of consent, or unacceptable or cumulative toxicity occurs.
Intravenous infusion.
Intravenous infusion.
Kokeellinen: Part 2 (Dose Expansion): PM54 + Pembrolizumab
Participants will receive recommended dose of PM54 in combination with pembrolizumab as observed in Part 1 of the study.
Intravenous infusion.
Intravenous infusion.

Mitä tutkimuksessa mitataan?

Ensisijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Parts 1 and 2: Number of Participants with Treatment-Emergent Adverse Events (TEAEs), Serious TEAEs and TEAEs Leading to Treatment Discontinuation
Aikaikkuna: From signing of the informed consent up to 30 days after last dose (up to 3 years)
From signing of the informed consent up to 30 days after last dose (up to 3 years)
Part 1: Number of Participants with Dose-Limiting Toxicities (DLTs)
Aikaikkuna: Cycle 1 (each cycle is of 21 days)
Cycle 1 (each cycle is of 21 days)
Part 2: Clinical Benefit Rate
Aikaikkuna: up to 12 weeks
CBR is defined as the percentage of participants who achieve either an objective tumor response - complete response (CR), partial response (PR) - or confirmed stable disease with an absence of tumor progression during the first 12 weeks. CBR was assessed according to modified Response Evaluation Criteria in Solid Tumors (mRECIST) v1.1. CR: Disappearance of all non-nodal target lesions and reduction in short axis of pathological lymph nodes to less than (<) 10 millimeter (mm); PR: at least a 30 percent (%) decrease in the sum of diameters of target lesions from baseline; SD: neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for progression disease (PD).
up to 12 weeks
Part 2: Objective Response Rate
Aikaikkuna: Baseline up to 3 years
ORR is defined as the percentage of participants who achieve complete response (CR) or partial response (PR) according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 as determined by the Investigator. CR: defined as disappearance of all target and all non-target lesions and no new lesions. PR: defined as at least a 30% decrease in sum of diameters of target lesions, taking as reference the baseline sum diameters, no progression of non-target lesions and no new lesions.
Baseline up to 3 years

Toissijaiset tulostoimenpiteet

Tulosmittaus
Toimenpiteen kuvaus
Aikaikkuna
Parts 1 and 2: Confirmed Objective Response Rate
Aikaikkuna: Baseline up to 3 years
Confirmed ORR is defined as a best objective response (OR) of CR or PR according to mRECIST v1.1 and determined by Investigator. CR: Disappearance of all non-nodal target lesions and reduction in short axis of pathological lymph nodes to < 10 mm; PR: at least a 30% decrease in the sum of diameters of target lesions from baseline.
Baseline up to 3 years
Part 1: Clinical Benefit Rate
Aikaikkuna: up to 12 weeks
CBR is defined as the percentage of participants who achieve either an objective tumor response - complete response (CR), partial response (PR) - or confirmed stable disease with an absence of tumor progression during the first 12 weeks. CBR was assessed according to mRECIST v1.1 and determined by Investigator. CR: Disappearance of all non-nodal target lesions and reduction in short axis of pathological lymph nodes to less than (<) 10 millimeter (mm); PR: at least a 30 percent (%) decrease in the sum of diameters of target lesions from baseline; SD: neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for progression disease (PD).
up to 12 weeks
Parts 1 and 2: Disease Control Rate (DCR)
Aikaikkuna: Baseline up to 3 years
DCR defined as the percentage of participants who achieve a best overall response of CR, PR and SD according to RECIST v1.1 and determined by Investigator. CR: defined as disappearance of all target and all non-target lesions and no new lesions. PR: defined as at least a 30% decrease in sum of diameters of target lesions, taking as reference the baseline sum diameters, no progression of non-target lesions and no new lesions. SD: SD: reduction in sum of diameters of target lesions of 10% or greater, confirmed on a subsequent scan.
Baseline up to 3 years
Parts 1 and 2: Progression-free survival (PFS)
Aikaikkuna: Baseline up to 3 years
Baseline up to 3 years
Parts 1 and 2: Duration of Response (DoR)
Aikaikkuna: Baseline up to 3 years
Baseline up to 3 years
Parts 1 and 2: Time to Treatment Failure
Aikaikkuna: Baseline up to 3 years
Baseline up to 3 years
Parts 1 and 2: Overall Survival (OS)
Aikaikkuna: Baseline up to 3 years
Baseline up to 3 years
Parts 1 and 2: Percentage of Participants who Achieve a Minor Response
Aikaikkuna: Baseline up to 3 years
Percentage of participants who achieve a minor response, defined as stable disease (per RECIST v1.1) with a reduction in sum of diameters of target lesions of 10% or greater, confirmed on a subsequent scan.
Baseline up to 3 years
Parts 1 and 2: Plasma Concentration of PM54 and Pembrolizumab
Aikaikkuna: Part 1- Cycle 1, Days 1 to 3: Pre-dose and at 1, 3, 6, 24 and 48 hours post-dose; Part 2- Cycle 1, Days 1 to 3: Pre-dose and at 1 and 48 hours post-dose (each cycle is 21 days)
Part 1- Cycle 1, Days 1 to 3: Pre-dose and at 1, 3, 6, 24 and 48 hours post-dose; Part 2- Cycle 1, Days 1 to 3: Pre-dose and at 1 and 48 hours post-dose (each cycle is 21 days)

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Opintojen ennätyspäivät

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Maanantai 8. kesäkuuta 2026

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Maanantai 8. kesäkuuta 2026

Ensimmäinen Lähetetty (Todellinen)

Perjantai 12. kesäkuuta 2026

Tutkimustietojen päivitykset

Viimeisin päivitys julkaistu (Todellinen)

Torstai 30. heinäkuuta 2026

Viimeisin lähetetty päivitys, joka täytti QC-kriteerit

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Viimeksi vahvistettu

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Lisää tietoa

Tähän tutkimukseen liittyvät termit

Muita asiaankuuluvia MeSH-ehtoja

Muut tutkimustunnusnumerot

  • PM54-A-003-25
  • 2025-523774-16 (Muu tunniste: EuCT Number)

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