Symptoms and General Pathology

All Conditions

Neoplasms

Blood and Lymph Conditions

Immune System Diseases

Infections

Heart and Blood Diseases

Rare Diseases

Syndrome

Lymphoma

Leukemia

Precursor Cell Lymphoblastic Leukemia-Lymphoma

Leukemia, Lymphoid

Hematologic Neoplasms

Leukemia, Myeloid

Leukemia, Myeloid, Acute

Leukemia, Lymphocytic, Chronic, B-Cell

Leukemia, Myelogenous, Chronic, BCR-ABL Positive

Lymphoma, Mantle-Cell

Lymphoma, Follicular

Lymphoma, B-Cell, Marginal Zone

Preleukemia

Myelodysplastic Syndromes

Burkitt Lymphoma

Waldenstrom Macroglobulinemia

Lymphoma, Non-Hodgkin

Neoplasms by Histologic Type

Lymphoproliferative Disorders

Lymphatic Diseases

Immunoproliferative Disorders

Hematologic Diseases

Bone Marrow Diseases

Leukemia, B-Cell

Chronic Disease

Disease Attributes

Lymphoma, B-Cell

Myeloproliferative Disorders

Communicable Diseases

Epstein-Barr Virus Infections

Virus Diseases

Herpesviridae Infections

DNA Virus Infections

Tumor Virus Infections

Neoplasms, Plasma Cell

Hemostatic Disorders

Blood Coagulation Disorders

Vascular Diseases

Paraproteinemias

Blood Protein Disorders

Hemorrhagic Disorders

Myeloid Leukemia

Acute Myeloid Leukemia

Lymphosarcoma

Acute Lymphoblastic Leukemia

Lymphoblastic Lymphoma

Chronic Graft Versus Host Disease

Acute Non Lymphoblastic Leukemia

Chronic Lymphocytic Leukemia

Chronic Myeloid Leukemia

Mantle Cell Lymphoma

Follicular Lymphoma

Marginal Zone Lymphoma

Acute Graft Versus Host Disease

B-cell Lymphoma

Chronic Myeloproliferative Disorders

HSC835

Novartis Pharmaceuticals

This study evaluated the safety and tolerability of using HSC835 in patients with hematological malignancies.

Safety and Tolerability of HSC835 in Patients With Hematological Malignancies

A First-in-human, Single-arm, Single-center, Open-label, Proof-of-concept Study to Evaluate the Safety and Tolerability of Infusing HSC835 (LFU835-expanded Umbilical Cord Blood Hematopoietic Stem Cells) in Patients With Hematological Malignancies

The safety and tolerability of HSC835 for clinical use were measured by infusional toxicity and absence of graft failure in excess of that currently observed with UCBT. Infusional toxicity - AE from transplant until first 48 hours. Administration of the HSC835 expanded CD34-positive cell product, infused over a period of approximately 15 minutes may theoretically cause adverse reactions based on hemodynamic effects, the release of factors like cytokines through administration into the systemic circulation, or acute hypersensitivity, among others.

Neutrophil recovery (engraftment) is defined as the first of three consecutive days with ANC \> 0.5 x 109/L which occurred for all patients before 42 days post transplant.

Incidence of platelet recovery within six months. Number of participants recovering platelet to ≥50,000 × 109/L for at least one week without transfusion in the prior 7 days to the first measurement.

Frequency of expanded unit predominance at day 100 (DUCBT recipients only) unit predominance was assessed by differences in microsatellite patterns between the recipient, HSC835 and the unmanipulated cord blood unit. Evaluation of sorted CD15-positive/CD33-positive myeloid and CD3-positive T cells in the peripheral blood, revealed three patterns: predominance of HSC835, Mixed dominance an unique chimerism pattern was observed with the CD15/CD33 population predominantly derived from HSC835 and the CD3 population almost exclusively derived from the unmanipulated unit, and predominance of the unmanipulated unit

Number of participants with incidence of transplant related mortality (TRM) within 100 days and one year

Number of participants with incidence of Acute Graft Versus Host Disease (aGVHD) within 100 days and Chronic Graft Versus Host Disease (cGVHD) within 1 year

Number of participants with Incidence of relapse within one year

Number of participants with Overall survival (OS) within one year

Number of participants with Disease Free Survival (DFS) within one year. Patients are considered to have achieved DFS or relapse-free survival if they had not experienced either relapse or death (of any cause)

Single umbilical cord blood transplant(SUCBT) less than 18 yrs

SUCBT < 18 Yrs

Single umbilical cord blood transplant (SUCBT) greater than or equal to 18 yrs

SUCBT >= 18 Yrs

Double umbilical cord blood transplant (DUCBT) less than 18 yrs

DUCBT < 18 Yrs

Double umbilical cord blood transplant (DUCBT) greater than or equal to 18 yrs

DUCBT >= 18 Yrs

Single umbilical cord blood transplant (SUCBT) This is the combination of the SUCBT\<18 yrs and SUCBT \>= 18 yrs

SUCBT

Double umbilical cord blood transplant (DUCBT) This is the combination of the DUCBT\<18 yrs and DUCBT \>= 18 yrs

DUCBT

Total

Age, Continuous

Sex: Female, Male

Study Director

Infusional Toxicity 48 hrs after transplant

Absence of graft failure after 32 days

Safety Analysis Set (SAS) comprising all patients who were transplanted is used for analysis of all demographic, safety and engraftment outputs.

Safety and Tolerability of HSC835 for Clinical Use Were Measured by Infusional Toxicity (Within First 48 Hours After Transplant) and Absence of Graft Failure After 32 Days in Excess of That Currently Observed With UCBT.

Incidence of Neutrophil Recovery Within 42 Days

Incidence of Platelet Recovery Within Six Months

Predominance of HSC835

Mixed dominance

Predominance of the unmaninpulated unit

Frequency of Expanded Unit Predominance at Day 100 (DUCBT Recipients Only)

Day 100

Month 12

Incidence of Transplant Related Mortality (TRM) Within 100 Days and One Year

aGVHD-Day 100

cGVHD-Month12

Incidence of Acute Graft Versus Host Disease (aGVHD) Within 100 Days and Chronic Graft Versus Host Disease (cGVHD) Within 1 Year

Incidence of Relapse Within One Year

Overall Survival (OS) Within One Year

Disease Free Survival (DFS) Within One Year

Overall Study

Multiple Myeloma

Patients with hematologic malignancies requiring UCB transplant with a NMA conditioning regimen.

HSC835 is a stem cell therapy product providing a source of Hematopoietic stem cell (HSC).

This study was designed to evaluate the safety and tolerability of HSC835 for clinical use as measured by the absence of graft failure at day 42 in excess of that currently observed with double umbilical cord blood (UCB) transplantation (DUCBT) with non-myeloablative (NMA) conditioning.

Safety and Tolerability of HSC835 in Patients With Hematological Malignancies Undergoing Single Umbilical Cord Blood Transplant

A Single-arm, Open-label Study to Evaluate the Safety and Tolerability of Infusing HSC835 in Patients With Hematological Malignancies Undergoing UCB Transplantation Using a Non-myeloablative Conditioning Regimen

Novartis is committed to sharing with qualified external researchers, access to patient-level data and supporting clinical documents from eligible studies. These requests are reviewed and approved by an independent review panel on the basis of scientific merit. All data provided is anonymized to respect the privacy of patients who have participated in the trial in line with applicable laws and regulations.

This trial data availability is according to the criteria and process described on www.clinicalstudydatarequest.com

This endpoint was to study safety and tolerability of HSC835 as measured by the absence of graft failure at day 42 in excess of that currently observed with double umbilical cord blood (UCB) transplantation (DUCBT) with non-myeloablative (NMA) conditioning.

Engraftment is defined as the first of three consecutive days with ANC \> 0.5 x 109/L.

NRM includes all patients who died from any other cause except relapse of the underlying disease during the study duration.

Overall survival is the proportion of patients who were alive at the end of the one year study period.

Patients are considered to have achieved relapse-free survival if they had not experienced either relapse or death (of any cause) at the end of the study.

Adverse events that occurred within the first 48 hours of transplant.

Time Period From Transplant Until 48hrs After Transplant

Adverse Events that occurred 48 hours post-transplant.

Time Period From Day 3 up to End of Study

Safety Analysis Set: The Safety analysis included all enrolled patients who were transplanted with HSC835 (any patient with a date for HSC835 transplant).

Study title	NCT ID	Conditions	Interventions	Eligibility	Organization	Link
Safety and Tolerability of HSC835 in Patients With Hematological Malignancies	NCT01474681	Acute Myelocyti... Acute Lymphocyt... Chronic Myeloge... Myelodysplastic... Chronic Lymphoc... Marginal Zone L... Follicular Lymp... Large-cell Lymp... Lymphoblastic L... Burkitt's Lymph... High Grade Lymp... Mantle-cell Lym... Lymphoplasmacyt...	HSC835	10 Years - 55 Years	Novartis
Safety and Tolerability of HSC835 in Patients With Hematological Malignancies Undergoing Single Umbilical Cord Blood Transplant	NCT01930162	Single Umbilica... Non-myeloablati... Acute Lymphocyt... Myelodysplastic... Non-Hodgkin's L... Multiple Myelom... Chronic Lymphoc...	HSC835	-	Novartis

Spots Global Cancer Trial Database for hsc835

Every month we try and update this database with for hsc835 cancer trials from around the world to help patients and their families find trials that might be right for them.
We offer this 100% free of charge and do not endorse any of the trials listed here, we hope it helps you or a loved one.

Spots Global Cancer Trial Database for hsc835

Every month we try and update this database with for hsc835 cancer trials from around the world to help patients and their families find trials that might be right for them. We offer this 100% free of charge and do not endorse any of the trials listed here, we hope it helps you or a loved one.

Every month we try and update this database with for hsc835 cancer trials from around the world to help patients and their families find trials that might be right for them.
We offer this 100% free of charge and do not endorse any of the trials listed here, we hope it helps you or a loved one.