Study of PM54 in Combination With Immunotherapy in Adult Participants With Advanced Malignancies
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
調査の概要
研究の種類
入学 (推定)
段階
- フェーズ2
- フェーズ 1
連絡先と場所
研究連絡先
- 名前:Cristian Fernandez, M.D.
- 電話番号:0034 91 846 6077
- メール:cmfernandez@pharmamar.com
研究場所
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New York
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New York、New York、アメリカ、11042
- 募集
- START New York
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Texas
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Fort Worth、Texas、アメリカ、76104
- 募集
- START Dallas
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Houston、Texas、アメリカ、77030
- 募集
- The University of Texas MD Anderson Cancer Center
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Houston、Texas、アメリカ、77054
- 募集
- NEXT Houston
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Irving、Texas、アメリカ、75039
- 募集
- NEXT Dallas
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Virginia
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Fairfax、Virginia、アメリカ、22031
- 募集
- NEXT Virginia
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Barcelona、スペイン
- まだ募集していません
- Institut Catala D'oncologia
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Madrid、スペイン
- 募集
- Hospital General Universitario Gregorio Marañón
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Madrid、スペイン
- 募集
- Clinica Universidad de Navarra (Cun)
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Madrid、スペイン
- 募集
- START Madrid - Hospital Universitario Fundacion Jimenez D
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Pamplona、スペイン
- 募集
- Clinica Universidad de Navarra (Cun)
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参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- Voluntarily signed and dated written informed consent, obtained before the start of any study-specific procedures.
- 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.
- Have a pathologically confirmed diagnosis of advanced malignancy.
- 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.
- Have measurable disease according to RECIST1.1 (or mRECIST v1.1 where applicable).
- 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.
- Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) of 0 or 1 at screening.
Individuals with central nervous system (CNS) metastases are eligible, as long as all of the following are met:
- Asymptomatic or minimally symptomatic and stable, with no worsening symptoms in the 4 weeks prior to start of study intervention.
- Does not require systemic corticosteroids in excess of an equivalent prednisone dose of 5 milligrams per day (mg/day).
- 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.
- 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.
Adequate laboratory parameters, as specified below, within 7 days of start of study intervention:
- 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).
- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) less than or equal to [<=] 3.0*the upper limit of normal (ULN).
- Total bilirubin <=1.0*ULN; up to 1.5*ULN for participants with Gilbert's syndrome.
- Creatinine clearance >=30 milliliter per minute (mL/min), calculated using the Cockcroft and Gault's formula.
- Serum albumin >=3 g/dL. Albumin infusion to increase the blood level in order to fulfill this inclusion criterion is strictly forbidden.
- Creatine kinase <=2.5*ULN.
- Recovered from the effects of any prior surgery or radiation.
- 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.
- Is willing to undergo trial procedures as specified in the protocol, including provision of biologic samples, as well as any study restrictions.
- 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:
- Prior treatment with PM54 or any other ecteinascidin agent, including ecubectedin, trabectedin, and lurbinectedin.
- History of hypersensitivity to PM54, pembrolizumab, or any of the inactive ingredients.
- 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.
- Presence of carcinomatous meningitis.
Presence of any of these medical conditions
Cardiovascular:
- History of myocardial, CNS, or other arterial infarction within 6 months before the start of study intervention.
- 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.
- Symptomatic arrhythmia or other significant electrocardiogram (ECG) abnormalities that in the opinion of the investigator pose an increased risk of complications.
Corrected QT interval (QTc) >470 milliseconds (ms) on the screening ECG or history of a long QT syndrome.
Respiratory
- History of interstitial lung disease (ILD) or pneumonitis that have required steroids or other forms of immunosuppression, or any ongoing or suspicion of ILD.
- 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.
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
- 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.
- 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.
- 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.
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:
- Traditional Chinese or herbal medicine with the intent to treat cancer or with known effects on drug metabolism: 28 days.
- Live, attenuated vaccines: 30 days.
- Chemotherapy: 21 days.
- Antibodies and antidrug conjugates: 28 days.
- Targeted agents and small molecules: 2 weeks or 5 half-lives, whichever is longer.
- 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.
- Whole-brain radiation therapy, stereotactic therapy, palliative radiation for symptom control and minor impact on bone marrow: 2 weeks.
- Other radiation therapy: 4 weeks.
- 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.
- Strong or moderate inhibitors or inducers of cytochrome (CYP) 3A4: 2 weeks.
- 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.
Active HIV infection. Inclusion is allowed if:
- Undergoing adequate anti-viral treatment and regular clinical oversight with good compliance.
- Undetectable human immunodeficiency virus (HIV) viral load.
- CD4+ lymphocyte count over 350 per millimeter cube.
- 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.
- Individuals with detectable hepatitis C virus (HCV) ribonucleic acid (RNA), which should be tested in case of positive anti-HCV antibody test.
- 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.
- Individuals with a short-term risk of anatomic complications from involvement of critical structures such as major vessels, large airways, and vertebral spine.
- 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).
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:非ランダム化
- 介入モデル:順次割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
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実験的: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.
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Intravenous infusion.
Intravenous infusion.
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実験的: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.
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Intravenous infusion.
Intravenous infusion.
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
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Parts 1 and 2: Number of Participants with Treatment-Emergent Adverse Events (TEAEs), Serious TEAEs and TEAEs Leading to Treatment Discontinuation
時間枠:From signing of the informed consent up to 30 days after last dose (up to 3 years)
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From signing of the informed consent up to 30 days after last dose (up to 3 years)
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Part 1: Number of Participants with Dose-Limiting Toxicities (DLTs)
時間枠:Cycle 1 (each cycle is of 21 days)
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Cycle 1 (each cycle is of 21 days)
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Part 2: Clinical Benefit Rate
時間枠:up to 12 weeks
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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).
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up to 12 weeks
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Part 2: Objective Response Rate
時間枠:Baseline up to 3 years
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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.
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Baseline up to 3 years
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Parts 1 and 2: Confirmed Objective Response Rate
時間枠:Baseline up to 3 years
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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.
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Baseline up to 3 years
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Part 1: Clinical Benefit Rate
時間枠:up to 12 weeks
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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).
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up to 12 weeks
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Parts 1 and 2: Disease Control Rate (DCR)
時間枠:Baseline up to 3 years
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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.
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Baseline up to 3 years
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Parts 1 and 2: Progression-free survival (PFS)
時間枠:Baseline up to 3 years
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Baseline up to 3 years
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Parts 1 and 2: Duration of Response (DoR)
時間枠:Baseline up to 3 years
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Baseline up to 3 years
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Parts 1 and 2: Time to Treatment Failure
時間枠:Baseline up to 3 years
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Baseline up to 3 years
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Parts 1 and 2: Overall Survival (OS)
時間枠:Baseline up to 3 years
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Baseline up to 3 years
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Parts 1 and 2: Percentage of Participants who Achieve a Minor Response
時間枠:Baseline up to 3 years
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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.
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Baseline up to 3 years
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Parts 1 and 2: Plasma Concentration of PM54 and Pembrolizumab
時間枠: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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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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協力者と研究者
スポンサー
出版物と役立つリンク
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- PM54-A-003-25
- 2025-523774-16 (その他の識別子:EuCT Number)
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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