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Neuroimmunological Disease
Neuromuscular Disease
Neurodegenerative Disease
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The list of conference materials is a subset of Roche/Genentech posters and oral presentations for the products that have data presented at the AAN 2026 conference. To browse full Roche/Genentech congress presentations and posters: Visit Medically.
Links to these presentations and posters will be added after the conference.
Genentech’s pipeline for Neuroscience includes multiple molecules currently under investigation.
These compounds and their uses are investigational and have not been approved by the U.S. Food and Drug Administration. This information is presented only for purposes of providing a general overview of clinical trials and should not be construed as a recommendation for use of any product for unapproved uses.
Exploring the pathophysiology of MS and the pivotal role of BTK in chronic central nervous system inflammation.
An introduction to Brainshuttle™ technology, an innovative platform that utilizes transferrin receptors to transport large therapeutic molecules across the blood-brain barrier.
These compounds and their uses are investigational and have not been approved by the U.S. Food and Drug Administration. This information is presented only for purposes of providing a general overview of clinical trials and should not be construed as a recommendation for use of any product for unapproved uses.
| Ocrelizumab | |||
|---|---|---|---|
| Indication | Phase | Trial Name | |
| Multiple Sclerosis | Phase II | A Study to Assess Bioequivalence of Two Subcutaneous (SC) Formulations of Ocrelizumab in Participants With Multiple Sclerosis (MS) (PORTAMENTO) | Visit trial |
| Fenebrutinib | |||
|---|---|---|---|
| Indication | Phase | Trial Name | |
| Multiple Sclerosis | Phase II | A Pharmacokinetics (PK), Pharmacodynamics (PD), Safety and Tolerability Study of Fenebrutinib in Children and Adolescents With Relapsing Multiple Sclerosis (RMS) (FENerations1) | Visit trial |
| RO7121932 | |||
|---|---|---|---|
| Indication | Phase | Trial Name | |
| Multiple Sclerosis | Phase I | A Study to Investigate the Safety, Tolerability, and Processing by the Body of Intravenous and Subcutaneous RO7121932 in Participants With Multiple Sclerosis (B-Shuttle) | Visit trial |
| P-CD19CD20-ALLO1 | |||
|---|---|---|---|
| Indication | Phase | Trial Name | |
| Multiple Sclerosis | Phase I | A Phase I, Multicenter, Open-Label Study to Evaluate the Safety, Tolerability, Cellular Kinetics, and Pharmacodynamics of P-CD19CD20-ALLO1 in Patients With Multiple Sclerosis | Visit trial |
| Satralizumab | |||
|---|---|---|---|
| Indication | Phase | Trial Name | |
| Autoimmune Encephalitis | Phase III | A Study to Evaluate the Efficacy, Safety, Pharmacokinetics (PK), and Pharmacodynamics (PD) of Satralizumab in Participants With Anti-N-methyl-D-aspartic Acid Receptor (NMDAR) or Anti-leucine-rich Glioma-inactivated 1 (LGI1) Encephalitis (Cielo) | Visit trial |
| NMOSD | Phase III | A Study To Evaluate Pharmacokinetics, Efficacy, Safety, Tolerability, And Pharmacodynamics Of Satralizumab In Pediatric Patients With Aquaporin-4 Antibody Positive Neuromyelitis Optica Spectrum Disorder (NMOSD) (SAkuraSun) | Visit trial |
| MYELIN OLIGODENDROCYTE GLYCOPROTEIN ANTIBODY DISEASE | Phase III | A Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Satralizumab in Patients With Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (Meteoroid) | Visit trial |
| Risdiplam | |||
|---|---|---|---|
| Indication | Phase | Trial Name | |
| SMA | Phase II | A Study to Investigate the Pharmacokinetics and Safety of Risdiplam in Infants With Spinal Muscular Atrophy (PUPFISH) | Visit trial |
| SMA | Phase IV | A Phase IV Open-Label Study Evaluating the Effectiveness and Safety of Risdiplam Administered as an Early Intervention in Pediatric Patients With Spinal Muscular Atrophy After Gene Therapy (HINALEA 1) | Visit trial |
| SMA | Phase IV | A Phase IV Open-Label Study Evaluating the Effectiveness and Safety of Risdiplam Administered in Pediatric Patients With Spinal Muscular Atrophy Who Experienced a Plateau or Decline in Function After Gene Therapy (HINALEA 2) | Visit trial |
| SMA | Phase IV | An observational study to look at the effects of Evrysdi (risdiplam) on fertility in adult male with spinal muscular atrophy (MARLIN) | Visit trial |
| Prasinezumab | |||
|---|---|---|---|
| Indication | Phase | Trial Name | |
| Parkinson's disease | Phase III | A Study to Evaluate the Efficacy and Safety of Intravenous (IV) Prasinezumab in Participants With Early-Stage Parkinson's Disease (PARAISO) | Visit trial |
| Trontinemab | |||
|---|---|---|---|
| Indication | Phase | Trial Name | |
| Alzheimer's | Phase III | A Study of Trontinemab in Participants With Early Symptomatic Alzheimer's Disease (TRONTIER I) | Visit trial |
| Alzheimer's | Phase III | A Clinical Trial of Trontinemab in Participants With Early Symptomatic Alzheimer's Disease (TRONTIER II) | Visit trial |
| Alzheimer's | Phase III | Master Screening Study to Determine Individuals With Potential Trial Eligibility for Alzheimer's Disease Studies as Assessed by Biomarker Status and Cognition (TRAVELLER) | Visit trial |
Interested in becoming an investigator or have trial questions?
Streamlining the Alzheimer’s diagnostic pathway: The role of biomarkers in ensuring accurate diagnosis and improving access to treatment.
This brochure details the PARAISO Phase III clinical trial, a study sponsored by Roche to evaluate the efficacy and safety of intravenous Prasinezumab in patients with early-stage Parkinson's disease
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You can find out more about your selected topic at Medically, a different Genentech Medical website which includes information about investigational compounds and uses. The information presented does not imply US FDA approval and should not be construed as a recommendation for use. Do you wish to proceed?
You can find out more about your selected topic at Medically, a different Genentech Medical website which includes information about investigational compounds and uses. The information presented does not imply US FDA approval and should not be construed as a recommendation for use. Do you wish to proceed?
You can find out more about your selected topic at Medically, a different Genentech Medical website which includes information about investigational compounds and uses. The information presented does not imply US FDA approval and should not be construed as a recommendation for use. Do you wish to proceed?
You can find out more about your selected topic at Medically, a different Genentech Medical website which includes information about investigational compounds and uses. The information presented does not imply US FDA approval and should not be construed as a recommendation for use. Do you wish to proceed?
You can find out more about your selected topic at Medically, a different Genentech Medical website which includes information about investigational compounds and uses. The information presented does not imply US FDA approval and should not be construed as a recommendation for use. Do you wish to proceed?
You can find out more about your selected topic at Medically, a different Genentech Medical website which includes information about investigational compounds and uses. The information presented does not imply US FDA approval and should not be construed as a recommendation for use. Do you wish to proceed?
You can find out more about your selected topic at Medically, a different Genentech Medical website which includes information about investigational compounds and uses. The information presented does not imply US FDA approval and should not be construed as a recommendation for use. Do you wish to proceed?
You can find out more about your selected topic at Medically, a different Genentech Medical website which includes information about investigational compounds and uses. The information presented does not imply US FDA approval and should not be construed as a recommendation for use. Do you wish to proceed?
You can find out more about your selected topic at Medically, a different Genentech Medical website which includes information about investigational compounds and uses. The information presented does not imply US FDA approval and should not be construed as a recommendation for use. Do you wish to proceed?
You can find out more about your selected topic at Medically, a different Genentech Medical website which includes information about investigational compounds and uses. The information presented does not imply US FDA approval and should not be construed as a recommendation for use. Do you wish to proceed?
You can find out more about your selected topic at Medically, a different Genentech Medical website which includes information about investigational compounds and uses. The information presented does not imply US FDA approval and should not be construed as a recommendation for use. Do you wish to proceed?
You can find out more about your selected topic at Medically, a different Genentech Medical website which includes information about investigational compounds and uses. The information presented does not imply US FDA approval and should not be construed as a recommendation for use. Do you wish to proceed?
You can find out more about your selected topic at Medically, a different Genentech Medical website which includes information about investigational compounds and uses. The information presented does not imply US FDA approval and should not be construed as a recommendation for use. Do you wish to proceed?
You can find out more about your selected topic at Medically, a different Genentech Medical website which includes information about investigational compounds and uses. The information presented does not imply US FDA approval and should not be construed as a recommendation for use. Do you wish to proceed?
You can find out more about your selected topic at Medically, a different Genentech Medical website which includes information about investigational compounds and uses. The information presented does not imply US FDA approval and should not be construed as a recommendation for use. Do you wish to proceed?
You can find out more about your selected topic at Medically, a different Genentech Medical website which includes information about investigational compounds and uses. The information presented does not imply US FDA approval and should not be construed as a recommendation for use. Do you wish to proceed?
Ab: antibody
AE: adverse event
ASTCT: American Society for Transplantation and Cellular Therapy
CR: complete response
CRS: cytokine release syndrome
CT: computed tomography
CTCAE: Common Terminology Criteria for Adverse Events
DoR: duration of response
ECOG PS: Eastern Cooperative Oncology Group performance status
FL: follicular lymphoma
ICANS: immune effector cell-associated neurotoxicity syndrome
IRF: independent review facility
IV: intravenous
IQR: interquartile range
NCI CTCAE: National Center Institute Common Terminology Criteria for Adverse Events
NHL: non-Hodgkin lymphoma
ORR: objective response rate
PET: positron emission tomography
PFS: progression-free survival
PR: partial response
R/R: relapsed/refractory
SAE: serious adverse event
SD: stable disease
USPI: United States Prescribing Information
UTI: urinary tract infection
ADC: Antibody–drug conjugate
AE: Adverse event
ALT: Alanine aminotransferase
ASCO: American Society of Clinical Oncology
BC: Breast cancer
BMI: Body mass index
C: Cycle
CAP: College of American Pathologists
CCOD: Clinical cutoff date
CDK4/6: Cyclin-dependent kinase 4 and 6
CDx: Companion diagnostic test
CI: Confidence interval
CKD-EPI: Chronic Kidney Disease Epidemiology Collaboration
CTCAE v4.03: Common Terminology Criteria for Adverse Events version 4.03
CTCAE v4: Common Terminology Criteria for Adverse Events version 4
CTCAE v5.0: Common Terminology Criteria for Adverse Events version 5.0
CTCAE: Common Terminology Criteria for Adverse Events
ctDNA: Circulating tumor DNA
D: Day
DOR: Duration of response
DPP-4: Dipeptidyl peptidase-4
ECOG PS: Eastern Cooperative Oncology Group performance status
eGFR: Estimated glomerular filtration rate
ER: Endocrine receptor
ESMO: European Society for Medical Oncology
ESO: European School of Oncology
ET: Endocrine therapy
FDA: Food and Drug Administration
Fulv: Fulvestrant
HbA1c: Hemoglobin A1c
HCP: Health care provider/professional
HER2: Human epidermal growth factor receptor 2
HR: Hazard ratio or hormone receptor, depending on context
i: Inhibitor
IM: Intramuscular
Inavo: Inavolisib
IV: Intravenous
mBC: Metastatic breast cancer
MedDRA: Medical Dictionary for Regulatory Activities
MTD: Maximum tolerated dose
mTOR: Mammalian target of rapamycin
mut: Mutated
NCI: National Cancer Institute
NGS: Next-generation sequencing
ORR: Overall response rate
OS: Overall survival
Palbo: Palbociclib
PARP: Poly (ADP-ribose) polymerase
Pbo: Placebo
PCR: Polymerase chain reaction
PD: Progressive disease
PFS: Progression-free survival
PgR: Progesterone receptor
PI3K: Phosphatidylinositol 3-kinase
PIK3CA: Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha
PK: Pharmacokinetics
PO: By mouth
PRO: Patient-reported outcome
Q#W: Every # weeks
Q4W: Every 4 weeks
QD: Daily
R: Randomized
RECIST v1.1: Response Evaluation Criteria In Solid Tumors version 1.1
SAE: Serious adverse event
SGLT2: Sodium-glucose co-transporter 2
SOC: Standard of care
T: Type
ULN: Upper limit of normal
USPI: United States Prescribing Information
CD3: Cluster of differentiation 3
TCR: T-cell receptor
CD4: Cluster of differentiation 4
CD8: Cluster of differentiation 8
CD226: Cluster of differentiation 226
Ig: Immunoglobulin
ITIM: Immunoreceptor tyrosine-based inhibitory motif
MHC: Major histocompatibility complex
NK: Natural killer
PD-1: Programmed cell death protein 1
PD-L1: Programmed death-ligand 1
PVR: Poliovirus receptor
TIGIT: T-cell immunoreceptor with Ig and ITIM domains
ASTCT: American Society for Transplantation and Cellular Therapy
CD20: Cluster of differentiation 20
CR: Complete response
CRS: Cytokine release syndrome
CT: Computed tomography
CTCAE: Common Terminology Criteria for Adverse Events
DLBCL: Diffuse large B-cell lymphoma
DoCR: Duration of complete response
DoR: Duration of response
ECOG PS: Eastern Cooperative Oncology Group performance status
FL: Follicular lymphoma
HGBCL: High-grade B-cell lymphoma
ICANS: Immune effector cell-associated neurotoxicity syndrome
IRC: Independent Review Committee
NOS: Not otherwise specified
ORR: Objective response rate
PET: Positron emission tomography
PMBCL: Primary mediastinal B-cell lymphoma
AE: Adverse event
Ang2: Angiopoietin-2
ASTCT: American Society for Transplantation and Cellular Therapy
ATG: Anti-thymocyte globulin
CAR: Chimeric antigen receptor
CARTOX: CAR T-cell Therapy-Associated Toxicity
CD3: Cluster of differentiation 3
CPAP: Continuous positive airway pressure
CRP: C-reactive protein
CRS: Cytokine release syndrome
CTCAE: Common Terminology Criteria for Adverse Events
DIC: Disseminated intravascular coagulation
HLH: Hemophagocytic lymphohistiocytosis
ICANS: Immune effector cell–associated neurotoxicity syndrome
ICU: Intensive care unit
IFN-γ: Interferon-gamma
IL: Interleukin
INR: International normalized ratio
IRR: Infusion-related reaction
MAS: Macrophage activation syndrome
MSKCC: Memorial Sloan Kettering Cancer Center
NO: Nitric oxide
PTT: Partial thromboplastin time
TNF-α: Tumor necrosis factor alpha
VWF: von Wilebrand factor
AAAAI: American Academy of Allergy Asthma & Immunology
DMT: Disease-modifying therapy
HCP: Health Care Provider
Ig: Immunoglobulin
LLN: Lower limit of normal
MS: Multiple Sclerosis
NK: Natural killer
ACTRIMS: Americas Committee for Treatment and Research in Multiple Sclerosis
CMSC: Consortium of Multiple Sclerosis Centers
ECTRIMS: European Committee for Treatment and Research in Multiple Sclerosis
FAERS: FDA Adverse Event Reporting System
FDA: US Food and Drug Administration
Ig: Immunoglobulin
LMP: last menstrual cycle
MCA: major congenital anomalies
MS: Multiple sclerosis
OCR: OCREVUS (ocrelizumab)
PML: progressive multifocal leukoencephalopathy
PPMS: Primary progressive multiple sclerosis
RMS: Relapsing multiple sclerosis
CD19: Cluster of differentiation 19
CD20: Cluster of differentiation 20
CDC: Centers for Disease Control and Prevention
COVID-19: Coronavirus disease of 2019
DMT: Disease-modifying therapy
ECTRIMS: European Committee for Treatment and Research in Multiple Sclerosis
EMA: European Medicines Association
FDA: Food and Drug Administration
IgG1: Immunoglobulin G1
LMP: Last menstrual period
mAb: Monoclonal antibody
MCA: Major congenital anomalies
MS: Multiple sclerosis
OCR: OCREVUS (ocrelizumab)
RID: Relative infant dose
UCSF: University of California San Francisco
URTI: Upper respiratory tract infection
UTI: Urinary tract infection
ADA: antidrug antibody
AE: adverse event
AUC: area under the serum concentration–time curve
CCOD: clinical cut-off date
CI: confidence interval
Cmax: maximum serum concentration
CTCAE: Common Terminology Criteria for Adverse Events
EDSS: Expanded Disability Status Scale
Gd+: gadolinium-enhancing
GMR: geometric mean ratio
h: hour
IR: injection reaction
IV: intravenous
LIR: local injection reaction
LLOQ: lower limit of quantification
MedDRA: Medical Dictionary for Regulatory Activities
min: minutes
MRI: magnetic resonance imaging
MS: multiple sclerosis
N/A: not applicable
N/E: new/enlarging
OCR: ocrelizumab
PD: pharmacodynamic
PDR: protocol-defined relapse
PK: pharmacokinetics
PPMS: primary progressive multiple sclerosis
PRO: patient-reported outcome
rHuPH20: recombinant human hyaluronidase PH20
RMS: relapsing multiple sclerosis
RoA: route of administration
SC: subcutaneous
SIR: systemic injection reaction
Tmax: time to maximum concentration
USPI: United States Prescribing Information
W: week
ABC: activated B-cell–like subtype
BICR: blinded independent central review
CI: confidence interval
CNS: central nervous system
CR: complete response
DLBCL: diffuse large B-cell lymphoma
ECOG PS: Eastern Cooperative Oncology Group performance status
EFSefficacy: event-free survival for efficacy causes (time from randomization to the earliest occurrence of disease progression/relapse, death due to any cause, initiation of any non-protocol specified anti-lymphoma treatment, or biopsy-confirmed residual disease after treatment completion)
EOT: end of treatment
GCB: germinal-center B-cell–like subtype
HGBL: high-grade B-cell lymphoma
HHV8: human herpesvirus 8
HR: hazard ratio
INV: investigator
IPI: International Prognostic Index
ITT: intention-to-treat
LYSA: Lymphoma Study Association
NE: not evaluable
NOS: not otherwise specified
OS: overall survival
PET-CT: positron emission tomography and computed tomography
PFS: progression-free survival
Pola-R-CHP: polatuzumab plus rituximab, cyclophosphamide, doxorubicin, prednisone
R: randomization
R-CHOP: rituximab plus cyclophosphamide, doxorubicin, vincristine, prednisone
R-CHP: rituximab plus cyclophosphamide, doxorubicin, prednisone
USPI: United States Prescribing Information
ARR: Annualized Relapse Rate
ART: Assisted Reproductive Technology
CI: Confidence Interval
DMT: Disease-modifying therapy
EDSS: Expanded Disability Status Scale
MS: Multiple Sclerosis
T: Trimester
OR: Odds ratio
OB/Gyn: Obstetrics and Gynecology
DBPCFC: Double-blind, placebo-controlled food challenge
FDA: Food and Drug Administration
ICH: International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use
IgE: Immunoglobulin E
NIH: National Institutes of Health
OIT: Oral immunotherapy
OLE: Open-label extension
R: Randomized
Streamlining the Alzheimer’s diagnostic pathway: The role of biomarkers in ensuring accurate diagnosis and improving access to treatment.
Exploring the pathophysiology of MS and the pivotal role of BTK in chronic central nervous system inflammation.
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