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GRACE: A Phase 1/2a Study of VTRU200 in Relapsed/Refractory AML, High-risk MDS, DLBCL Post CART Failure and Advanced Solid Tumors

3. August 2026 aktualisiert von: Vitruviae

A Phase I/IIa Dose Escalation and Expansion Study of VTRU200 in Adult and Pediatric Participants With Relapsed/Refractory AML, HR-MDS, DLBCL Post-CART Failure and Advanced Solid Tumors

About this study

This is the first study of VTRU200 in people. The main purpose of this study is to find a safe dose of VTRU200 and learn how the medicine behaves in the body. Researchers will also look for early signs that it may help treat cancer.

VTRU200 is an experimental immunotherapy. It is designed to help the body's immune system find and destroy cancer cells while limiting effects on healthy cells.

Unlike many cancer treatments that target a single protein, VTRU200 recognizes stress signals that are commonly found on cancer cells. These signals include certain sugars (called glycans) and fats (called phospholipids) that are present on many types of cancer cells but are uncommon on normal healthy cells. VTRU200 also attaches to immune cells called T cells and helps direct them to attack cancer cells.

Because VTRU200 targets features that are shared by many cancers, it may continue to work even if cancer cells lose or change individual proteins that other treatments depend on.

Who can take part?

This study is for people with certain blood cancers that have come back after treatment or have not responded to available treatments. These include:

Acute myeloid leukemia (AML) Higher-risk myelodysplastic syndromes (HR-MDS) Diffuse large B-cell lymphoma (DLBCL) that has returned after CAR T-cell therapy

Later parts of the study may also include adolescents and children with AML.

What will happen during the study?

Participants will receive VTRU200 through a vein (intravenous infusion).

The study will begin by giving small doses to help determine the safest dose for future participants. If those doses are well tolerated, later participants may receive higher doses.

Researchers will:

Monitor participants closely for side effects. Perform blood tests to measure how VTRU200 moves through and leaves the body. Measure how the immune system responds to treatment. Check whether the cancer shrinks, disappears, or remains under control.

Participants may receive multiple treatment cycles if they continue to benefit and do not have unacceptable side effects.

What are the possible benefits?

VTRU200 may or may not help participants. Information learned from this study may help develop new treatments for people with these cancers in the future.

What are the possible risks?

Because VTRU200 is being tested in humans for the first time, not all side effects are known.

Possible risks include reactions related to activation of the immune system, infusion-related reactions, laboratory test changes, and other side effects. Participants will be monitored closely throughout the study, and medical care will be available if side effects occur.

Brief Study Description

This first-in-human, open-label, Phase 1/2a study will evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, immunogenicity, and preliminary antitumor activity of VTRU200 in participants with relapsed or refractory acute myeloid leukemia (AML), higher-risk myelodysplastic syndromes (HR-MDS), or diffuse large B-cell lymphoma (DLBCL) following CAR T-cell therapy. VTRU200 is an investigational trispecific T-cell engager that binds stress-associated glycans, phosphatidylserine, and CD3 to redirect T cells toward cancer cells. The Phase 1 dose-escalation portion will determine the recommended Phase 2 dose (RP2D), followed by disease-specific expansion cohorts to further evaluate safety and preliminary antitumor activity.

Why is this research important?

Many blood cancers eventually stop responding to available treatments. Cancer cells can escape therapy by changing or losing the proteins that many current medicines target.

VTRU200 is designed to recognize stress-related features that many cancer cells share rather than relying on a single protein target. Researchers hope this approach may reduce the chance of treatment resistance while limiting damage to healthy cells. This study will help determine whether VTRU200 can be given safely and whether it shows early signs of helping people with difficult-to-treat blood cancers.

Studienübersicht

Detaillierte Beschreibung

Relapsed or refractory (R/R) acute myeloid leukemia (AML), higher-risk myelodysplastic syndromes (HR-MDS), and diffuse large B-cell lymphoma (DLBCL) after chimeric antigen receptor (CAR) T-cell therapy remain associated with poor clinical outcomes despite recent therapeutic advances. Although targeted therapies and immunotherapies have improved outcomes for some patients, treatment failure frequently occurs because of disease heterogeneity, antigen loss, immune escape, and treatment resistance. Therefore, novel therapeutic approaches capable of recognizing shared cancer-associated features across genetically diverse tumors are needed.

VTRU200 is a first-in-class, investigational trispecific T-cell engager (TCE) designed to redirect endogenous T cells toward malignant cells through simultaneous binding of CD3 on T cells and two stress-associated tumor surface markers: aberrant high-mannose glycans and phosphatidylserine (PS). These glycan and lipid structures are enriched on many malignant cells and cells within the tumor microenvironment as a consequence of altered glycosylation, metabolic stress, oxidative stress, endoplasmic reticulum stress, impaired membrane asymmetry, rapid proliferation, and resistance to therapy. In contrast, these targets are minimally exposed on most normal healthy tissues, providing the rationale for selective tumor targeting.

Preclinical studies demonstrated that VTRU200 binds tumor cells expressing these stress-associated surface markers and mediates potent T-cell activation and cytotoxicity across multiple AML models. In nonclinical studies, VTRU200 exhibited antitumor activity in vitro and in vivo, demonstrated minimal cytokine release relative to conventional CD3-engaging therapies, showed no detectable binding to normal human peripheral blood leukocytes or hematopoietic stem and progenitor cells, and did not bind an FDA-recommended panel of normal human or cynomolgus monkey tissues. Repeat-dose animal studies demonstrated a favorable therapeutic window supporting clinical evaluation.

This is a first-in-human, multicenter, open-label Phase 1/2a study evaluating the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), immunogenicity, and preliminary antitumor activity of VTRU200 administered by intravenous infusion.

The Phase 1 dose-escalation portion will determine the maximum tolerated dose (MTD), if reached, and identify the recommended Phase 2 dose (RP2D). Dose escalation will begin with an accelerated titration design using sentinel participants at the lowest dose levels, followed by a Bayesian Optimal Interval (BOIN) design after evidence of acceptable safety. Escalation decisions will be based on predefined safety criteria and review by the Safety Review Committee.

Following determination of the RP2D, the Phase 2a dose-expansion portion will further characterize the safety profile and evaluate preliminary clinical activity in disease-specific cohorts. Adult participants with R/R AML and HR-MDS will constitute the primary efficacy population, with additional exploratory cohorts enrolling participants with DLBCL following CAR T-cell therapy failure. Adolescent and pediatric participants with AML may be enrolled after establishment of an acceptable safety profile and appropriate adult exposure.

Safety evaluations will include monitoring of adverse events, serious adverse events, infusion-related reactions, immune-mediated toxicities including cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS), clinical laboratory testing, vital signs, electrocardiograms, physical examinations, and concomitant medications.

PK assessments will characterize serum concentrations of VTRU200, while immunogenicity assessments will evaluate anti-drug antibodies (ADA). PD analyses will assess biomarkers of immune activation, cytokine responses, target engagement, and changes within peripheral blood and bone marrow, where applicable.

Preliminary antitumor activity will be evaluated using disease-specific response criteria, including the European LeukemiaNet (ELN) recommendations for AML, International Working Group (IWG) criteria for HR-MDS, and Lugano Classification criteria for DLBCL. Additional efficacy endpoints include measurable residual disease (MRD), duration of response, progression-free survival, overall survival, and other clinically relevant measures of disease control.

This study is designed primarily to establish the safety profile, appropriate dose, and biologic activity of VTRU200 while providing an initial assessment of its clinical activity in patients with relapsed or refractory hematologic malignancies for whom effective treatment options remain limited.

Studientyp

Interventionell

Einschreibung (Geschätzt)

108

Phase

  • Phase 2
  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Kind
  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

Inclusion Criteria:

  • 1. Adults (≥18 years) with

I. Pathologically confirmed acute myeloid leukemia (AML) according to WHO 2022 criteria. Relapsed or refractory AML, defined as either:

  1. Refractory AML: Failure to achieve CR, CRh, or CRi after at least 2 courses of intensive induction therapy.
  2. Relapsed AML: Recurrence after prior CR, CRh, or CRi, documented by one or more of the following: Bone marrow blasts >5% by morphologic assessment; persistent reappearance of blasts in peripheral blood by morphologic assessment II. HR-MDS: Pathologically confirmed myelodysplastic syndrome (MDS) according to WHO 2022 criteria, with high-risk disease defined as IPSS-R high-risk or very high-risk (score >4.5). Ineligible for allogeneic hematopoietic stem cell transplantation.

III. DLBCL post-CAR T: histologically confirmed DLBCL per WHO 2022 criteria and relapsed or refractory disease after prior CART therapy. Qualifying post-CAR T treatment failure must be documented at least 1 month after CAR T infusion and include no metabolic response, first metabolic progressive disease, or first relapse after prior response. Prior CART infusion must have occurred at least 1 month before screening. Participants must not be in partial metabolic response or complete metabolic response at screening and must have measurable disease on PET/CT (preferred) or CT/MRI, defined as at least 1 nodal lesion >1.5 cm or at least 1 extranodal lesion >1.0 cm; if PET is used, lesions must be FDG-avid and consistent with active lymphoma IV. Advanced solid tumors 2. Children (6 months-11 years) and adolescents (12-17 years) with R/R-AML.

  1. Children and adolescent refractory AML: Bone marrow contains 1% blasts by multiparametic flow cytometry (MFC) at the end of 2 cycles of induction therapy
  2. Children and adolescent relapsed AML: A single bone marrow sample showing 5% leukemic blasts by MFC, fluorescence in situ hybridization (FISH) testing or other molecular method, or a single bone marrow sample with at least two tests showing 1% blasts such as by MFC, karyotypic abnormality with at least one metaphase similar or identical to diagnosis, FISH abnormality identical to one present at diagnosis (above level of sensitivity of specific FISH probe) or polymerase chain reaction (PCR) or next generation sequencing (NGS)-based demonstration of leukemogenic lesion (e.g., fusion, mutation) identical to diagnosis and is quantifiably 1% 3. Eastern Cooperative Oncology Group (ECOG) performance status 0-2 or Karnofsky Performance Score (KPS) ≥50% 4. Adequate organ function: I. Hepatic: Serum AST/ALT ≤2.5×ULN and total bilirubin ≤1.5×ULN (≤3×ULN if Gilbert's syndrome) II. Renal: Serum creatinine ≤1.5×ULN; Calculated CrCl: ≥40 mL/min (Cockcroft-Gault [adults]; Schwartz formula [adolescents]; apply if serum creatinine is borderline) III. Cardiac: ejection fraction ≥ 50% and no evidence of pericardial effusion as determined by ECHO IV. Hematologic: WBC count must be ≤20 × 10⁹/L prior to the first dose of study treatment and before each dose in Cycle 1; patients with WBC >20 × 10⁹/L may receive cytoreduction with hydroxyurea (up to 4 g/day) and/or leukapheresis per protocol to achieve this threshold, with hydroxyurea held ≥12-24 hours before each study treatment dose 5. Females of childbearing potential must have a negative serum or urine pregnancy test 6. Adults: written informed consent. Adolescents: written patient assent plus parental/guardian informed consent.

    7. Prior treatment with an investigational agent is permitted provided that at least 5 half-lives have elapsed and all treatment-related toxicities have resolved to Grade ≤1 (except alopecia). Prior T-cell engaging, checkpoint inhibitor, or cellular therapies require a minimum washout of 8 weeks.

    Exclusion Criteria:

    • 1. Active central nervous system (CNS) disease requiring treatment. 2. Uncontrolled or clinically significant baseline neurologic disorder (e.g., uncontrolled seizures or severe cognitive impairment/delirium), significant psychiatric illness or active substance abuse.

      3. Uncontrolled infections including persistent bacteremia/fungemia despite appropriate therapy, progressive invasive fungal infection, or uncontrolled viral infection with end-organ disease. Active tuberculosis.

      4. Concurrent malignancy requiring active systemic therapy. 5. Cytotoxic chemotherapy within 14 days prior to first dose. Targeted anti-leukemic therapy within 7-14 days prior to first dose. Radiotherapy within 14 days prior to first dose (except limited-field palliative radiotherapy). Prior CD3-engaging therapy.

      6. T-cell depleting therapy (ATG, alemtuzumab, or equivalent) within 6 months prior to enrollment 7. Severe uncontrolled cardiovascular disease (e.g., NYHA class III/IV heart failure, unstable angina or MI within 6 months, uncontrolled arrhythmia). Severe uncontrolled pulmonary disease (e.g., requiring high-flow oxygen or ventilatory support).

      8. Systemic corticosteroids >10 mg/day prednisone equivalent within 7 days prior to first dose.

      9. Active autoimmune disease requiring systemic immunosuppression within the past 12 months.

      10. Prior allogeneic transplant within 3 months or active graft-versus-host disease (GVHD).

      11. Primary immunodeficiency (congenital immunodeficiency disorder requiring ongoing medical management).

      12. Known HIV infection. Hepatitis B: HBsAg positive (chronic HBV infection). Hepatitis C: anti-HCV positive (HCV exposure).

      13. Pregnant or breastfeeding 14. Known congenital or acquired bleeding disorder, including hemophilia A/B or von Willebrand disease, or other clinically significant coagulopathy 15. History of severe allergic reaction to immunotherapy

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Sequenzielle Zuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Arm A
ARM A: Adult R/R AML and HR-MDS; VTRU200 infusion
VTRU200 is an investigational humanized trispecific T-cell engager administered by intravenous infusion. It binds CD3 on T cells and tumor associated glycans and lipids to redirect T-cell cytotoxicity toward malignant cells. Multiple dose levels will be evaluated during dose escalation to determine safety and the recommended Phase 2 dose.
Experimental: ARM B
Adult DLBCL post-CAR T failure; VTRU200 infusion
VTRU200 is an investigational humanized trispecific T-cell engager administered by intravenous infusion. It binds CD3 on T cells and tumor associated glycans and lipids to redirect T-cell cytotoxicity toward malignant cells. Multiple dose levels will be evaluated during dose escalation to determine safety and the recommended Phase 2 dose.
Experimental: ARM C
Adolescent R/R AML with no curative option (12-17 years); VTRU200 infusion
VTRU200 is an investigational humanized trispecific T-cell engager administered by intravenous infusion. It binds CD3 on T cells and tumor associated glycans and lipids to redirect T-cell cytotoxicity toward malignant cells. Multiple dose levels will be evaluated during dose escalation to determine safety and the recommended Phase 2 dose.
Experimental: ARM D
Expansion at RP2D-Adult R/R AML and HR-MDS; VTRU200 infusion
VTRU200 is an investigational humanized trispecific T-cell engager administered by intravenous infusion. It binds CD3 on T cells and tumor associated glycans and lipids to redirect T-cell cytotoxicity toward malignant cells. Multiple dose levels will be evaluated during dose escalation to determine safety and the recommended Phase 2 dose.
Experimental: ARM E
Expansion at RP2D: Adult DLBCL post-CAR T failure
VTRU200 is an investigational humanized trispecific T-cell engager administered by intravenous infusion. It binds CD3 on T cells and tumor associated glycans and lipids to redirect T-cell cytotoxicity toward malignant cells. Multiple dose levels will be evaluated during dose escalation to determine safety and the recommended Phase 2 dose.
Experimental: ARM F
Expansion at RP2D: Adolescent R/R AML with no curative option; VTRU200 infusion
VTRU200 is an investigational humanized trispecific T-cell engager administered by intravenous infusion. It binds CD3 on T cells and tumor associated glycans and lipids to redirect T-cell cytotoxicity toward malignant cells. Multiple dose levels will be evaluated during dose escalation to determine safety and the recommended Phase 2 dose.
Experimental: ARM G
Expansion at RP2D: Adult solid cancers; VTRU200 infusion
VTRU200 is an investigational humanized trispecific T-cell engager administered by intravenous infusion. It binds CD3 on T cells and tumor associated glycans and lipids to redirect T-cell cytotoxicity toward malignant cells. Multiple dose levels will be evaluated during dose escalation to determine safety and the recommended Phase 2 dose.
Experimental: ARM H
Expansion at RP2D: Pediatric R/R AML (6 months-11 years) ; VTRU200 infusion
VTRU200 is an investigational humanized trispecific T-cell engager administered by intravenous infusion. It binds CD3 on T cells and tumor associated glycans and lipids to redirect T-cell cytotoxicity toward malignant cells. Multiple dose levels will be evaluated during dose escalation to determine safety and the recommended Phase 2 dose.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Phase 1: Safety and tolerability
Zeitfenster: 28 days
Incidence and severity of treatment-emergent AEs (number and percentage)
28 days
Phase 1: Safety and tolerability
Zeitfenster: 28 days
Incidence of serious adverse events (number and percentage)
28 days
Phase 1: Pharmacokinetics
Zeitfenster: 6 months
6 months
Phase 1: Safety and tolerability
Zeitfenster: 28 days
Incidence of dose-limiting toxicities
28 days
Phase 1: Determination of RP2D
Zeitfenster: 6 months
Integrated assessment of safety, PK, PD and preliminary disease-specific evidence of biological activity (e.g., reduction in bone marrow blast percentage, peripheral blood blast clearance, hematologic recovery, or reduction in measurable tumor burden
6 months
Phase 2a: Efficacy
Zeitfenster: 12 months
Adult AML: Durable CR and durable CR+CRh (ELN criteria)
12 months
Phase 2a: Efficacy
Zeitfenster: 12 months
HR-MDS: Durable CR and CR+PR (IWG criteria)
12 months
Phase 2a: Efficacy
Zeitfenster: 12 months
DLBCL: ORR (Lugano Classification)
12 months
Phase 2a- Preliminary Efficacy
Zeitfenster: 12 months
Advanced solid tumors: ORR (RECIST v1.1)
12 months

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Phase 2a: Safety and tolerability
Zeitfenster: 24 months
Treatment-emergent adverse events (Incidence and percentage)
24 months
Phase 1: Preliminary Efficacy
Zeitfenster: 6 months
Complete remission (CR) rate in AML
6 months
Phase 1- Preliminary Efficacy
Zeitfenster: 6 months
Composite overall response rate (ORR = CR + CRh + CRi + MLFS + PR) in AML
6 months
Phase 1- Preliminary Efficacy
Zeitfenster: 6 months
Minimal residual disease (MRD) negativity rate (<0.01%) in AML
6 months
Phase 1- Preliminary Efficacy
Zeitfenster: 24 months
Duration of response (DoR) in AML responders
24 months
Phase 1- Preliminary Efficacy
Zeitfenster: 6 months
Complete remission (CR) rate in high-risk MDS
6 months
Phase 1- Preliminary Efficacy
Zeitfenster: 6 months
Overall response rate in high-risk MDS
6 months
Phase 1- Preliminary Efficacy
Zeitfenster: 24 months
Duration of response (DoR) in high-risk MDS
24 months
Phase 1- Preliminary Efficacy
Zeitfenster: 6 months
Overall response rate (ORR) in DLBCL
6 months
Phase 1- Preliminary Efficacy
Zeitfenster: 6 months
Duration of response (DoR) in DLBCL
6 months
Phase 1- Preliminary Efficacy
Zeitfenster: 6 moths
Overall response rate (ORR) in advanced solid tumors
6 moths
Phase 1- Preliminary Efficacy
Zeitfenster: 6 months
Disease control rate (DCR) in advanced solid tumors
6 months
Phase 1- Preliminary Efficacy
Zeitfenster: 24 months
Duration of response (DoR) in advanced solid tumors
24 months
Phase 1- Preliminary Efficacy
Zeitfenster: 6 months
Composite overall response rate (ORR) in pediatric AML
6 months
Phase 1- Preliminary Efficacy
Zeitfenster: 6 months
Minimal residual disease (MRD) negativity rate (<0.01%) in pediatric AML
6 months
Phase 1- Incidence of Anti-drug Antibodies
Zeitfenster: 6 months
Incidence of Anti-drug Antibodies
6 months
Phase 1- Preliminary Efficacy
Zeitfenster: 6 months
Complete remission (CR) rate in AML
6 months
Phase 2a: Safety and tolerability
Zeitfenster: 24 months
Treatment-related adverse events (Incidence and percentage)
24 months
Phase 2a: Safety and tolerability
Zeitfenster: 24 months
Serious adverse events (Incidence and percentage)
24 months
Phase 2a- Efficacy
Zeitfenster: 6 months
Composite overall response rate (ORR = CR + CRh + CRi + MLFS + PR) in AML
6 months

Andere Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Phase 2a- Exploratory
Zeitfenster: 24 months
Change from baseline in tumor-reactive T-cell clonal expansion
24 months
Phase 2a- Exploratory
Zeitfenster: 24 months
Persistence of tumor-reactive T-cell clones
24 months
Phase 2a- Exploratory
Zeitfenster: 24 months
Change from baseline in PD-1 expression
24 months
Phase 2a- Exploratory
Zeitfenster: 24 months
Change from baseline in IDO1 expression
24 months
Phase 2a- Exploratory
Zeitfenster: 24 months
Change from baseline in myeloid-derived suppressor cell (MDSC) frequency
24 months
Phase 2a- Exploratory
Zeitfenster: 24 months
Change from baseline in regulatory T-cell (Treg) frequency
24 months
Phase 2a- Exploratory
Zeitfenster: 24 months
Change from baseline in extracellular vesicle phosphatidylserine (PS) expression
24 months
Phase 2a- Exploratory
Zeitfenster: 24 months
Change from baseline in extracellular vesicle high-mannose glycan (Man9) expression
24 months

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. Januar 2027

Primärer Abschluss (Geschätzt)

1. Januar 2028

Studienabschluss (Geschätzt)

1. Januar 2029

Studienanmeldedaten

Zuerst eingereicht

29. Juli 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

3. August 2026

Zuerst gepostet (Tatsächlich)

6. August 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

6. August 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

3. August 2026

Zuletzt verifiziert

1. August 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Plan für individuelle Teilnehmerdaten (IPD)

Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?

UNENTSCHIEDEN

Beschreibung des IPD-Plans

The sponsor has not yet determined whether de-identified individual participant data (IPD) collected during this study will be shared with other researchers. Any future data-sharing decisions will consider participant privacy, informed consent, applicable laws and regulations, protection of confidential and proprietary information, and scientific and regulatory considerations.

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Ja

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .

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