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Neoantigen Peptide Vaccine Plus Pembrolizumab in Renal Cell Carcinoma (NPVPP)

29 giugno 2026 aggiornato da: Jian Lin

A Phase I Clinical Trial of Personalized Neoantigen Peptide Vaccine in Combination With Pembrolizumab for the Safety and Efficacy in Patients With Advanced, Recurrent or Refractory Renal Cell Carcinoma

This is a Phase I, single-center, open-label, single-arm clinical trial to evaluate the safety and efficacy of personalized neoantigen polyepitope peptide vaccine combined with pembrolizumab in patients with advanced, recurrent or refractory renal cell carcinoma (RCC).

Background: Renal cell carcinoma is one of the most common malignancies of the urinary system. Although pembrolizumab has become a standard first-line treatment, the objective response rate (ORR) of monotherapy is only 20-40%, and most patients eventually develop primary or acquired resistance. Tumor neoantigens are specific antigens produced by tumor-specific gene mutations, with high immunogenicity and tumor specificity, making them ideal targets for tumor immunotherapy. Preliminary clinical studies have shown that neoantigen vaccines can produce synergistic effects when combined with pembrolizumab.

Study Design: This is an investigator-initiated trial (IIT) conducted at Peking University First Hospital. The study will enroll 5-8 patients in two stages: an initial safety assessment cohort (3 patients) followed by an expansion cohort (5 additional patients) if safety criteria are met. The study drug is a personalized neoantigen polyepitope peptide vaccine (Neo-RCC), produced by Mingzhibenyuan Medical Technology (Beijing) Co., Ltd., based on whole exome sequencing (WES) and transcriptome sequencing (RNA-seq) of each patient's tumor tissue. The vaccine is administered via subcutaneous injection in combination with Polyinosinic-polycytidylic acid stabilized with poly-L-lysine and carboxymethylcellulose (Poly-ICLC) adjuvant, with a priming phase (5 injections on Days 0, 3, 7, 14, 21) and a boosting phase (3 injections on Weeks 6, 12, and 20), totaling 8 injections. Pembrolizumab (200 mg intravenous [IV] every 3 weeks [Q3W]) is administered concurrently as combination therapy.

Primary Objective: To evaluate the safety of the personalized neoantigen peptide vaccine in advanced RCC patients, as measured by the incidence and severity of treatment-emergent adverse events (TEAE) graded by National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) v5.0.

Secondary Objectives: To evaluate pharmacokinetic characteristics; to assess efficacy including objective response rate (ORR), duration of response (DOR), disease control rate (DCR), progression-free survival (PFS), and overall survival (OS) per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1.

Key Eligibility Criteria: Adults (≥18 years) with Stage III or IV, locally advanced, recurrent or metastatic non-surgical RCC who have achieved disease stability for ≥3 months after prior targeted therapy combined with pembrolizumab; measurable disease per RECIST v1.1; Eastern Cooperative Oncology Group (ECOG) performance status 0-3; adequate organ function; and ≥50 tumor gene mutations detectable from biopsy tissue.

Safety Monitoring: A Data Safety Monitoring Board (DSMB) will oversee patient safety. Dose-limiting toxicities (DLT) are defined according to protocol-specified criteria. If ≥2 DLTs occur in the initial cohort, the adjuvant dose will be reduced by 50% and the study will proceed with a de-escalation cohort.

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Intervento / Trattamento

Descrizione dettagliata

Study Rationale: This study addresses the unmet need for effective second-line or later treatment options for advanced renal cell carcinoma (RCC) patients who have progressed or become refractory after initial immunotherapy. The combination strategy leverages the complementary mechanisms of personalized neoantigen vaccines (which activate tumor-specific T-cell responses) and pembrolizumab (which blocks programmed cell death protein 1 (PD-1)-mediated immune suppression), potentially overcoming PD-1 inhibitor resistance.

Neoantigen Prediction and Vaccine Manufacturing: Tumor tissue and peripheral blood samples are collected for whole exome sequencing (WES) and RNA sequencing (RNA-seq). A proprietary neoantigen prediction platform (neoTrue AI) analyzes sequencing data to identify tumor-specific mutations and predict neoantigen-major histocompatibility complex (MHC) binding affinity. The top 10-30 ranked neoantigen peptides are selected for Good Manufacturing Practice (GMP)-grade synthesis. The median manufacturing period is approximately 12 weeks. Each peptide is 300 μg, mixed with Polyinosinic-polycytidylic acid stabilized with poly-L-lysine and carboxymethylcellulose (Poly-ICLC) adjuvant (0.5 mg per pool), and administered as 4 pools (left/right axilla and left/right groin) in 250 μL per injection site.

Pembrolizumab Administration: Pembrolizumab 200 mg is administered intravenously (IV) every 3 weeks (Q3W), diluted in 100 mL 0.9% sodium chloride over 30 minutes. Treatment continues for up to 2 years or until disease progression, unacceptable toxicity, or patient withdrawal. During the vaccine manufacturing period (~12 weeks), pembrolizumab may be continued as bridging therapy to maintain disease stability.

Dose-Limiting Toxicity (DLT) Definition: Hematologic: Grade 4 neutropenia (absolute neutrophil count [ANC] <0.5×10⁹/L) lasting >7 days; Grade 4 thrombocytopenia (<25×10⁹/L) within 7 days. Non-hematologic: Grade 3 non-hematologic toxicity lasting >7 days (with specified exceptions); Grade 4 toxicity. Immune-related: ≥Grade 3 immune pneumonitis, colitis, hepatitis; any-grade myocarditis; ≥Grade 2 immune effector cell-associated neurotoxicity syndrome (ICANS) or immune encephalitis; ≥Grade 3 severe skin reactions (Stevens-Johnson syndrome/toxic epidermal necrolysis [SJS/TEN], drug reaction with eosinophilia and systemic symptoms [DRESS]). Other: ≥Grade 2 cytokine release syndrome (CRS) (per American Society for Transplantation and Cellular Therapy [ASTCT] criteria); ≥Grade 3 injection-site reactions requiring surgical intervention; ≥Grade 3 allergic reactions; ≥Grade 3 infections; ≥Grade 3 thromboembolic events; ≥Grade 3 bleeding.

DLT Management: If ≥2 DLTs occur in the first 3 patients during the first 8 weeks (D0-D56), the adjuvant total dose will be reduced by 50% (to 1.0 mg), and 2 additional patients will be enrolled in the de-escalation cohort. If ≥2 DLTs occur in the de-escalation cohort, the study will be terminated. If ≥3 DLTs occur in the expansion cohort, the regimen will be deemed to have unacceptable toxicity.

Efficacy Assessments: Tumor assessments by computed tomography (CT) or magnetic resonance imaging (MRI) per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 are conducted at screening, every 6-8 weeks during treatment, at treatment completion/early termination, and during follow-up. Blinded Independent Central Review (BICR) may be used as sensitivity analysis.

Pharmacokinetic/Immunogenicity Assessments: Peripheral blood mononuclear cells (PBMCs) are collected at baseline, 24-72 hours post-injection, every 2 treatment cycles, and at treatment completion. Neoantigen-specific T-cell responses are quantified by quantitative polymerase chain reaction (qPCR) for interferon-gamma (IFN-γ), tumor necrosis factor-alpha (TNF-α), interleukin-2 (IL-2), granzyme B, and perforin mRNA expression. T-cell receptor (TCR) sequencing is performed to track clonal expansion. Circulating tumor DNA minimal residual disease (ctDNA-MRD) monitoring panels are designed based on each patient's WES data and detected by targeted next-generation sequencing (NGS).

Follow-up Schedule: Long-term follow-up every 3 months for survival status and subsequent anti-tumor treatments.

Risk Mitigation: Comprehensive risk management plans are established for cytokine release syndrome (CRS), immune effector cell-associated neurotoxicity syndrome (ICANS), immune-related adverse events (irAEs), infections, injection-related reactions, adjuvant-related risks, pseudoprogression, hyperprogressive disease, and RCC-specific complications (paraneoplastic syndromes, hemorrhage, thromboembolism). A Data Safety Monitoring Board (DSMB) is constituted to oversee safety.

Funding: This study is supported by a research grant from the GenScript Life Science Research Grant Program (2024), with additional support from Mingzhibenyuan Medical Technology (Beijing) Co., Ltd. for neoantigen prediction and peptide synthesis.

Tipo di studio

Interventistico

Iscrizione (Stimato)

8

Fase

  • Fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

  • Nome: Jian Lin, Professor
  • Numero di telefono: +86 1380-1358-465
  • Email: linjianbj@163.com

Luoghi di studio

  • Cina
    • Beijing Municipality
      • Beijing, Beijing Municipality, Cina, 100034
        • Peking University First Hospital
        • Contatto:
          • Yinmo Yang, Professor
          • Numero di telefono: +86-10-83572211
          • Email: bdyyec@163.com

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  1. Histologically or cytologically confirmed Stage III or IV, locally advanced, recurrent or metastatic renal cell carcinoma (RCC) not amenable to curative surgery
  2. Disease stability for ≥3 months after prior single pembrolizumab therapy, with documented progression or intolerance to standard treatment
  3. At least one measurable lesion per RECIST v1.1 (longest diameter ≥10 mm for non-lymph node lesions; short axis ≥15 mm for lymph nodes; or bone lesions confirmed by CT/MRI)
  4. Age ≥18 years
  5. Estimated life expectancy ≥3 months
  6. ECOG performance status 0-3
  7. Availability of tumor tissue (biopsy or archival specimen) for whole exome sequencing (WES) and RNA sequencing (RNA-seq), with ≥50 tumor gene mutations detectable

  8. Adequate organ function as defined by laboratory parameters within 14 days prior to enrollment:

    8.1 Hematologic: Absolute Neutrophil Count(ANC) ≥1.5×10⁹/L, platelet count ≥100×10⁹/L, hemoglobin ≥90 g/L; 8.2 Hepatic: total bilirubin(TBIL) ≤1.5×Upper Limit of Normal(ULN), Aspartate Aminotransferase(AST)/Alanine Aminotransferase(ALT) ≤2.5×ULN (≤5×ULN if liver metastases present); 8.3 Renal: serum creatinine ≤1.5×ULN or creatinine clearance ≥50 mL/min (Cockcroft-Gault formula); 8.4 Coagulation: international normalized ratio(INR) ≤1.5, activated partial thromboplastin time(APTT) ≤1.5×ULN; 8.5 Cardiac: Left Ventricular Ejection Fractions(LVEF) ≥50% by echocardiography;

  9. Ability to comply with study procedures and follow-up schedule;
  10. Signed informed consent form;
  11. For women of childbearing potential: negative serum pregnancy test (Human Chorionic Gonadotropin sensitivity ≤25 IU/L) within 7 days prior to enrollment; agreement to use effective contraception during study and for 4 weeks after last dose;
  12. For men: agreement to use effective contraception during study and for 4 weeks after last dose.

Exclusion Criteria:

  1. Pregnant or lactating women

  2. Prior treatment with:

    2.1 Two or more lines of immune checkpoint inhibitor (ICI) systemic therapy; 2.2 CTLA-4 inhibitor (e.g., ipilimumab); 2.3 Tumor vaccine therapy (including neoantigen vaccine, dendritic cell vaccine, etc.); 2.4 Chemotherapy specifically for renal cell carcinoma; 2.5 Allogeneic hematopoietic stem cell or solid organ transplantation;

  3. Active autoimmune disease or other immune-mediated disorders requiring systemic immunosuppressive therapy;
  4. Participation in another investigational drug study within 4 weeks prior to first dose;

  5. Active infection including:

    5.1 Known Human Immunodeficiency Virus(HIV) infection; 5.2 Active hepatitis B (HBsAg positive and Hepatitis B Virus-DNA >500 IU/mL) or hepatitis C (HCV-RNA positive); 5.3 Active tuberculosis (T-SPOT or PPD positive with clinical symptoms, or chest CT suggestive of active TB); 5.4 Severe infection requiring intravenous antibiotics within 2 weeks prior to enrollment, or uncontrolled systemic infection;

  6. Symptomatic central nervous system (CNS) metastases; exception: patients with treated CNS metastases stable for ≥4 weeks without neurological symptoms and without corticosteroid requirement;

  7. Uncontrolled comorbidities including:

    7.1 Symptomatic congestive heart failure (New York Heart Association Class III-IV); 7.2 Unstable angina or myocardial infarction within 6 months; 7.3 Uncontrolled arrhythmia; 7.4 Uncontrolled hypertension (systolic ≥160 mmHg or diastolic ≥100 mmHg despite standard treatment); 7.5 Active peptic ulcer or gastrointestinal bleeding; 7.6 Active interstitial lung disease or pulmonary fibrosis;

  8. Other malignancy within 5 years (except cured cervical carcinoma in situ, basal cell carcinoma, or squamous cell skin carcinoma);
  9. Live vaccine administration within 4 weeks prior to enrollment or planned during study (inactivated vaccines allowed);
  10. Known hypersensitivity to peptide vaccine components, adjuvants (e.g., Montanide ISA-51, Poly-ICLC), or pembrolizumab;
  11. Sarcomatoid or rhabdoid RCC as predominant histology (mixed histology allowed if non-pure sarcomatoid/rhabdoid);
  12. Any condition that, in the investigator's opinion, would compromise patient safety or compliance;
  13. Any other condition that the investigator considers unsuitable for study participation.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Neo-RCC + Pembrolizumab
All enrolled patients receive the same experimental intervention: personalized neoantigen polyepitope peptide vaccine (Neo-RCC) combined with pembrolizumab. The neoantigen vaccine is individually designed based on whole exome sequencing (WES) and RNA sequencing of each patient's tumor tissue, synthesized as 10-30 peptides (300 μg each), mixed with Poly-ICLC adjuvant, and administered via subcutaneous injection at 4 sites (bilateral axilla and groin) over 8 injections (priming on Days 0, 3, 7, 14, 21; boosting on Weeks 6, 12, 20). Pembrolizumab 200 mg IV is administered every 3 weeks concurrently. Enrollment follows a two-stage design: initial safety cohort (n=3) followed by expansion cohort (n=5) if dose-limiting toxicity criteria are met.
Droga: Personalized Neoantigen Polyepitope Peptide Vaccine
This intervention consists of a personalized neoantigen polyepitope peptide vaccine (Neo-RCC) individually designed and manufactured for each patient based on whole exome sequencing (WES) and transcriptome sequencing (RNA-seq) of tumor tissue. The vaccine contains 10-30 synthetic long peptides (300 μg each) predicted to bind to the patient's Human Leukocyte Antigen(HLA), mixed with Poly-ICLC adjuvant (0.5 mg per pool). The total peptide dose is 4-9 mg per patient. Administration is via subcutaneous injection at 4 anatomical sites (bilateral axilla and bilateral groin) in 250 μL per site. The vaccination schedule includes a priming phase (5 injections on Days 0, 3, 7, 14, 21) and a boosting phase (3 injections on Weeks 6, 12, and 20), totaling 8 injections over approximately 20 weeks. The vaccine is administered in combination with pembrolizumab 200 mg intravenously every 3 weeks. Manufacturing is conducted under GMP conditions by Mingzhibenyuan Medical Technology (Beijing) Co., Ltd.
Altri nomi:
  • Neo-RCC

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Incidence and severity of treatment-emergent adverse events (TEAE)
Lasso di tempo: From first dose of study drug through 30 days after last dose, approximately 24 weeks
The primary safety endpoint is the incidence and severity of treatment-emergent adverse events (TEAE), graded according to NCI CTCAE v5.0. TEAE is defined as any adverse event that occurs from the first administration of the study drug through 30 days after the last dose, or before initiation of new anti-tumor therapy, whichever occurs first. Key assessments include: (1) overall TEAE incidence rate; (2) Grade ≥3 TEAE incidence rate; (3) serious adverse event (SAE) incidence rate; (4) adverse events of special interest (AESI) including immune-related adverse events (irAEs), injection-site reactions, and cytokine release syndrome; (5) TEAE leading to dose modification, interruption, or permanent discontinuation; (6) treatment-related death. Safety monitoring covers the screening period, treatment period (8 vaccine injections over ~20 weeks plus concurrent pembrolizumab), and follow-up period.
From first dose of study drug through 30 days after last dose, approximately 24 weeks

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Objective Response Rate (ORR) per RECIST v1.1
Lasso di tempo: From first dose through disease progression or death, up to 2 years
Objective Response Rate (ORR) is defined as the proportion of patients achieving best overall response of complete response (CR) or partial response (PR) according to RECIST v1.1 criteria. Tumor assessments are conducted by CT or MRI at screening, every 6-8 weeks during treatment, at treatment completion/early termination, and during follow-up. Blinded Independent Central Review (BICR) may be used as sensitivity analysis. ORR reflects the anti-tumor activity of the personalized neoantigen polyepitope peptide vaccine combined with pembrolizumab in advanced RCC patients.
From first dose through disease progression or death, up to 2 years
Duration of Response (DOR) per RECIST v1.1
Lasso di tempo: From first documented response to disease progression or death, up to 2 years
Duration of Response (DOR) is defined as the time from first documented CR or PR (whichever occurs first) to first documented disease progression (PD) per RECIST v1.1 or death from any cause, whichever occurs first. For patients who have not progressed or died at the time of analysis, DOR is censored at the last tumor assessment date.
From first documented response to disease progression or death, up to 2 years
Disease Control Rate (DCR) per RECIST v1.1
Lasso di tempo: From first dose through 6 weeks after first dose, up to 2 years
Disease Control Rate (DCR) is defined as the proportion of patients achieving best overall response of complete response(CR), partial response(PR), or stable disease (SD) with duration ≥6 weeks per RECIST v1.1 criteria.
From first dose through 6 weeks after first dose, up to 2 years
Progression-Free Survival (PFS) per RECIST v1.1
Lasso di tempo: From first dose to disease progression or death, up to 2 years
Progression-Free Survival (PFS) is defined as the time from first dose of study drug to first documented PD per RECIST v1.1 or death from any cause, whichever occurs first. Patients who have not progressed or died are censored at the last tumor assessment date.
From first dose to disease progression or death, up to 2 years
Overall Survival (OS)
Lasso di tempo: From first dose to death or last contact, up to 2 years
Overall Survival (OS) is defined as the time from first dose of study drug to death from any cause. Patients who are alive at the time of analysis are censored at the last known alive date.
From first dose to death or last contact, up to 2 years
Cmax of neoantigen-specific T-cell response
Lasso di tempo: From first dose through 30 days after last dose, approximately 24 weeks
Peak level of neoantigen-specific T-cell response in peripheral blood during treatment, measured by qPCR for IFN-γ, TNF-α, IL-2, granzyme B, perforin mRNA expression or TCR clonotype analysis. Peripheral blood mononuclear cells(PBMCs) collected at baseline, 24-72 hours post-injection, every 2 treatment cycles, and at treatment completion.
From first dose through 30 days after last dose, approximately 24 weeks
Tmax of neoantigen-specific T-cell response
Lasso di tempo: From first dose through 30 days after last dose, approximately 24 weeks
Time from first dose to peak level (Cmax) of neoantigen-specific T-cell response in peripheral blood, measured by qPCR for IFN-γ, TNF-α, IL-2, granzyme B, perforin mRNA expression or TCR clonotype analysis. PBMCs collected at baseline, 24-72 hours post-injection, every 2 treatment cycles, and at treatment completion.
From first dose through 30 days after last dose, approximately 24 weeks
Duration of neoantigen-specific T-cell response
Lasso di tempo: From first dose through 30 days after last dose, approximately 24 weeks
Time from first detectable neoantigen-specific T-cell response to return to baseline or below threshold, measured by qPCR for IFN-γ, TNF-α, IL-2, granzyme B, perforin mRNA expression or TCR clonotype analysis. PBMCs collected at baseline, 24-72 hours post-injection, every 2 treatment cycles, and at treatment completion.
From first dose through 30 days after last dose, approximately 24 weeks
Area under curve(AUC) of neoantigen-specific T-cell response
Lasso di tempo: From first dose through 30 days after last dose, approximately 24 weeks
Area under the T-cell response-time curve for neoantigen-specific immune response in peripheral blood, measured by qPCR for IFN-γ, TNF-α, IL-2, granzyme B, perforin mRNA expression or TCR clonotype analysis. PBMCs collected at baseline, 24-72 hours post-injection, every 2 treatment cycles, and at treatment completion.
From first dose through 30 days after last dose, approximately 24 weeks
Percent change from baseline in neoantigen-specific T-cell response
Lasso di tempo: From first dose through 30 days after last dose, approximately 24 weeks
Percent change from baseline at each timepoint for neoantigen-specific T-cell response in peripheral blood, measured by qPCR for IFN-γ, TNF-α, IL-2, granzyme B, perforin mRNA expression or TCR clonotype analysis. PBMCs collected at baseline, 24-72 hours post-injection, every 2 treatment cycles, and at treatment completion.
From first dose through 30 days after last dose, approximately 24 weeks

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Jian Lin

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Pubblicazioni generali

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 settembre 2026

Completamento primario (Stimato)

1 gennaio 2029

Completamento dello studio (Stimato)

1 settembre 2029

Date di iscrizione allo studio

Primo inviato

21 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

29 giugno 2026

Primo Inserito (Effettivo)

7 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

7 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

29 giugno 2026

Ultimo verificato

1 aprile 2026

Maggiori informazioni

Termini relativi a questo studio

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • PV-0001

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

SÌ

Criteri di accesso alla condivisione IPD

IPD and supporting information will be available to qualified researchers upon reasonable request. Interested researchers may contact the Principal Investigator or the study team at Peking University First Hospital to submit a data access request. The request should include a detailed research proposal outlining the scientific rationale, specific data requirements, and planned analyses. Access will be granted following review and approval by the study team, subject to compliance with applicable data protection regulations, patient confidentiality agreements, and institutional policies. De-identified individual participant data, along with the study protocol and statistical analysis plan, may be shared via a secure data transfer mechanism. Data access is contingent upon the execution of a data use agreement and is intended solely for non-commercial research purposes.

Tipo di informazioni di supporto alla condivisione IPD

  • STUDIO_PROTOCOLLO
  • LINFA
  • ICF
  • CODICE_ANALITICO
  • RSI

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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