Drug Monograph

Tofersen (Qalsody)

tofersen — antisense oligonucleotide

Antisense Oligonucleotide (ASO) — SOD1 mRNA-Targeting · Intrathecal Injection
Pharmacokinetic Profile
Effective Half-Life (CSF)
~4 weeks
Metabolism
Exonuclease hydrolysis (non-CYP)
Plasma Tmax
2–6 hours
Accumulation
Little to none after loading
CNS Distribution
Confirmed (autopsy tissue, n=3)
Clinical Information
Drug Class
Antisense Oligonucleotide (ASO)
Available Dose
100 mg/15 mL single-dose vial
Route
Intrathecal injection (lumbar puncture)
Renal Adjustment
Not studied (not expected to be needed)
Hepatic Adjustment
Not studied (non-hepatic metabolism)
Pregnancy
No adverse effects in animal studies
Lactation
Unknown; detected in mouse milk
Schedule / Legal Status
Rx only; Orphan Drug; Accelerated Approval
Generic Available
No
Genetic Testing Required
Yes — confirmed SOD1 mutation
Rx

Indications

IndicationApproved PopulationTherapy TypeStatus
ALS in patients with a SOD1 gene mutationAdults with confirmed SOD1 mutationDisease-modifying (gene-targeted); may be used alongside riluzole and/or edaravoneFDA Accelerated Approval

Tofersen is the first approved treatment targeting a specific genetic cause of ALS. It was granted accelerated approval in April 2023 based on reduction in plasma neurofilament light chain (NfL), a biomarker of axonal injury and neurodegeneration, rather than on a statistically significant change in a clinical functional measure. SOD1 mutations account for approximately 2% of all ALS cases and up to 20% of familial ALS. Continued approval may be contingent upon verification of clinical benefit in confirmatory trials, including the ongoing ATLAS study evaluating tofersen in presymptomatic SOD1 mutation carriers.

Off-Label / Investigational Uses

Presymptomatic SOD1 mutation carriers: The Phase 3 ATLAS trial (NCT04856982) is evaluating whether tofersen can delay clinical onset of ALS when initiated in presymptomatic individuals with SOD1 mutations and elevated NfL. Results are pending. Evidence quality: Low (ongoing trial, no completed data).

Dose

Dosing

Clinical ScenarioStarting DoseMaintenance DoseMaximum DoseNotes
SOD1-ALS — loading phase100 mg IT every 14 days × 3 doses100 mg IT every 28 days100 mg per administrationAdminister as 15 mL intrathecal bolus injection over 1–3 min via lumbar puncture. Remove ~10 mL CSF before injection.
Loading: Day 1, Day 15, Day 29. Maintenance begins Day 57.
SOD1-ALS — maintenance phase100 mg IT every 28 days100 mg per administrationContinue indefinitely. Maximal CSF trough concentration reached at third (last loading) dose. No accumulation with monthly maintenance dosing.
Administered by or under direction of HCPs experienced in lumbar punctures.
Missed dose — second loading doseAdminister ASAP; give third loading dose 14 days laterResume the original loading schedule from the missed dose.
Missed dose — third loading or any maintenance doseAdminister ASAP; next dose 28 days laterResume maintenance schedule from the missed dose.
Clinical Pearl: Intrathecal Administration

Tofersen requires lumbar puncture for each dose. Allow the refrigerated vial to warm to room temperature without external heat. Remove approximately 10 mL of CSF before injecting the full 15 mL (100 mg) as a bolus over 1–3 minutes. Consider sedation and/or imaging guidance based on the patient’s clinical condition. Administer within 4 hours of removing the solution from the vial. The drug contains no preservatives.

PK

Pharmacology

Mechanism of Action

Tofersen is a 20-mer 5-10-5 MOE gapmer antisense oligonucleotide designed to bind to SOD1 messenger RNA (mRNA). This binding triggers RNase H-mediated cleavage and degradation of the mRNA, thereby reducing synthesis of the superoxide dismutase 1 (SOD1) protein. In patients with SOD1-mutated ALS, gain-of-function mutations lead to production of a toxic, misfolded SOD1 protein that drives motor neuron degeneration. By reducing total SOD1 protein levels, tofersen aims to slow the neurodegenerative process at its upstream genetic source. In the pivotal trial, tofersen reduced CSF SOD1 protein by approximately 35% and plasma NfL by approximately 55% at 28 weeks, providing pharmacodynamic evidence of target engagement and reduced neurodegeneration.

ADME Profile

ParameterValueClinical Implication
Absorption / DistributionIT administration into CSF; distributes from CSF to CNS tissues (confirmed by autopsy in 3 patients); transfers from CSF to plasma with Tmax 2–6 hDirect CNS delivery bypasses the blood-brain barrier; systemic exposure is a secondary consequence of CSF clearance, not the therapeutic target
CSF KineticsMaximum CSF trough at third dose (end of loading); little to no accumulation during monthly maintenance; effective CSF half-life ~4 weeksLoading phase is critical for achieving steady-state CNS exposure; monthly maintenance maintains trough levels
MetabolismExonuclease (3′- and 5′)-mediated hydrolysis; not a substrate/inhibitor/inducer of CYP450 enzymes or major transportersNo hepatic CYP metabolism means negligible risk of drug-drug interactions and no need for hepatic dosing adjustments
EliminationPrimary route not characterised; no plasma accumulation with monthly dosingThe ~4-week CSF half-life supports the monthly maintenance dosing interval; renal/hepatic impairment studies have not been conducted
SE

Side Effects

≥10%Very Common
Adverse EffectIncidenceClinical Note
Pain (includes back pain, pain in extremity)42% (vs 22% placebo)Most common AE; largely procedural (lumbar puncture-related). Post-LP pain management with analgesics and hydration; consider lying flat post-procedure
Fatigue17% (vs 6% placebo)May overlap with ALS-related fatigue; assess whether temporally related to dosing days
Arthralgia14% (vs 6% placebo)Joint pain, often mild; manage with standard analgesics if needed
CSF white blood cell increased14% (vs 0% placebo)Pleocytosis; reflects CSF inflammatory response to ASO administration. Usually asymptomatic. Distinguish from infectious meningitis or myelitis
Myalgia14% (vs 6% placebo)Muscle pain; may occur systemically post-dose
5–10%Common
Adverse EffectIncidenceClinical Note
CSF protein increased8% (vs 3% placebo)Reflects intrathecal inflammatory response; monitor in context of clinical symptoms
Musculoskeletal stiffness6% (vs 0% placebo)Often mild and self-limiting
Neuralgia6% (vs 0% placebo)Nerve pain; evaluate for radiculitis if persistent or severe
SeriousSerious (Regardless of Frequency)
Adverse EffectEstimated FrequencyTypical OnsetRequired Action
Myelitis and/or radiculitis~4% (6/147 patients)Variable; can occur after any doseInitiate diagnostic workup (MRI spine, CSF analysis); treat per standard of care; may require interruption or permanent discontinuation. 2 of 6 patients discontinued; remaining 4 resolved without stopping
Papilledema / elevated intracranial pressure~3% (4/147 patients)VariableFundoscopic exam; standard ICP management. All 4 patients resolved with treatment; none discontinued tofersen
Aseptic meningitis (chemical meningitis)~1% (2/147 patients)Hours to days post-doseCSF analysis to exclude infectious aetiology; supportive care. 1 patient discontinued tofersen; 1 continued treatment
DiscontinuationDiscontinuation Rates
Overall Enrolment into OLE
88% continued to open-label extension
Context: 95 of 108 participants from VALOR enrolled in the OLE, indicating high treatment acceptability despite intrathecal administration
Serious Neurological Events (Overall)
7% of tofersen-treated patients
Events: Myelitis, radiculitis, aseptic meningitis, elevated ICP, papilledema. Most were reversible; few led to treatment discontinuation
Managing Serious Neurological Events

All three categories of serious neurological adverse reactions (myelitis/radiculitis, elevated ICP/papilledema, aseptic meningitis) are class effects of intrathecal ASO administration. Clinical teams should have protocols in place for MRI spine, fundoscopy, and CSF analysis. Most events resolved with standard-of-care management and did not require permanent discontinuation. Symptoms of myelitis may include new or worsening limb weakness or sensory changes, which require careful differentiation from ALS disease progression.

Int

Drug Interactions

No clinical drug interaction studies have been performed with tofersen. As an antisense oligonucleotide administered intrathecally, tofersen is metabolised by exonuclease-mediated hydrolysis and is not a substrate, inhibitor, or inducer of CYP450 enzymes or major drug transporters. No clinically significant pharmacokinetic interactions are expected. In the VALOR trial, 62% of patients were taking concomitant riluzole and 8% were taking edaravone, with no apparent interaction signals.

MinorRiluzole
MechanismNo pharmacokinetic interaction expected; tofersen is metabolised by exonucleases, not CYP enzymes
Effect62% of VALOR participants used riluzole concurrently without interaction signals; NfL reductions consistent regardless of riluzole use
ManagementNo dose adjustment required; continue riluzole as clinically indicated
FDA PI / VALOR trial
MinorEdaravone
MechanismDifferent metabolic pathways (exonuclease vs UGT/sulfotransferases); different routes (IT vs IV/PO)
Effect8% of VALOR participants used edaravone concurrently without safety or efficacy signals
ManagementNo dose adjustment required
FDA PI / VALOR trial
MinorAnticoagulants / Antiplatelets
MechanismNo pharmacokinetic interaction; procedural consideration for lumbar puncture bleeding risk
EffectTheoretical increased risk of spinal/epidural haematoma with LP while anticoagulated
ManagementFollow standard LP guidelines regarding timing relative to anticoagulant/antiplatelet agents
Clinical practice / LP guidelines
Interaction Profile Summary

Tofersen has no known clinically significant drug-drug interactions. Its intrathecal route and non-CYP metabolism make pharmacokinetic interactions exceedingly unlikely. The primary procedural concern is the interaction between anticoagulant therapy and the need for repeated lumbar punctures, which is a well-established procedural consideration rather than a drug-drug interaction.

Mon

Monitoring

  • Neurological AssessmentBefore and after each dose
    Routine
    Evaluate for new neurological symptoms (limb weakness, sensory changes, vision changes, headache, neck stiffness) before and after each intrathecal injection. Differentiate drug-related myelitis/radiculitis from ALS progression.
  • Plasma NfLBaseline, then periodically
    Routine
    Plasma neurofilament light chain is the surrogate biomarker on which accelerated approval was based. Reductions of ~55% were observed at 28 weeks in the pivotal trial. Track to assess treatment response and guide shared decision-making.
  • ALSFRS-R ScoreBaseline, then every 1–3 months
    Routine
    Standard ALS functional outcome measure. The pivotal trial did not achieve statistical significance on this endpoint at 28 weeks, but long-term data at 148 weeks showed numerically less decline with earlier tofersen initiation.
  • Fundoscopic ExamBaseline, then periodically
    Trigger-based
    Papilledema and elevated intracranial pressure reported in 4 patients. Perform if patient reports visual changes, persistent headache, or nausea/vomiting post-dose.
  • CSF AnalysisAs clinically indicated
    Trigger-based
    If symptoms of myelitis, radiculitis, or meningitis develop, send CSF for cell count, protein, glucose, and culture to exclude infection. CSF pleocytosis and protein elevation are common with tofersen and do not necessarily indicate a serious neurological event.
  • SOD1 Genetic ConfirmationBefore first dose
    Routine
    A confirmed SOD1 mutation by a central or certified laboratory is required before initiating treatment. Tofersen is not indicated for ALS without a confirmed SOD1 mutation.
  • Coagulation StatusBefore each LP
    Routine
    Standard pre-LP assessment. Evaluate anticoagulant/antiplatelet use and platelet count. Follow institutional LP guidelines for timing of anticoagulant hold.
CI

Contraindications & Cautions

Absolute Contraindications

  • None listed in the FDA prescribing information. Tofersen has no formally listed contraindications. However, standard contraindications to lumbar puncture (raised ICP with mass lesion, local infection at puncture site, severe coagulopathy) apply to the administration procedure itself.

Relative Contraindications (Specialist Input Recommended)

  • Prior serious neurological event with tofersen: Patients who experienced myelitis, radiculitis, or aseptic meningitis requiring treatment discontinuation should be evaluated by a neurology specialist before considering rechallenge.
  • Active CNS infection: Intrathecal injection should be deferred until infection has resolved.
  • Significant coagulopathy or active anticoagulation: LP may be contraindicated or require careful timing; discuss with haematology if the patient requires ongoing anticoagulation.

Use with Caution

  • Pregnancy: No adverse developmental effects observed in animal studies (mice at 4x and rabbits at 20x human exposure). No adequate human data. Weigh risk-benefit.
  • Breastfeeding: Detected in mouse milk; human data unavailable. Consider risk-benefit.
  • Paediatric patients: Safety and efficacy not established in children.
  • Patients with prior lumbar surgery or spinal abnormalities: May require imaging-guided LP.
FDA Accelerated Approval — Safety Advisory Serious Neurological Events: Myelitis, Radiculitis, Papilledema, Aseptic Meningitis

Tofersen does not carry an FDA Boxed Warning. However, the Warnings and Precautions section highlights three categories of serious neurological events: (1) myelitis and/or radiculitis (6 patients; 2 required discontinuation); (2) papilledema and elevated intracranial pressure (4 patients; none discontinued); and (3) aseptic meningitis (2 patients; 1 discontinued). All events were reversible. Clinicians should monitor for new neurological symptoms and initiate diagnostic workup promptly. Management may require dose interruption or discontinuation.

Additionally, tofersen was approved under accelerated approval based on a surrogate biomarker (plasma NfL reduction). The primary clinical endpoint (ALSFRS-R change) did not reach statistical significance in the 28-week pivotal trial. Continued approval may be contingent upon confirmatory trial results.

Pt

Patient Counselling

Purpose of Therapy

Tofersen is designed to target the specific genetic cause of SOD1-mutated ALS by reducing the production of the toxic SOD1 protein. It was approved based on its ability to lower neurofilament light chain, a blood marker of nerve damage, rather than on a traditional clinical endpoint. Long-term data over approximately three years suggest that patients treated earlier may experience slower functional decline and prolonged survival compared to what is expected from the natural course of SOD1-ALS. However, tofersen does not cure ALS or restore lost motor function.

How Treatment Is Given

Tofersen is given as an injection into the spinal fluid (intrathecal injection) through a lumbar puncture, performed by a healthcare provider experienced in this procedure. Treatment begins with three loading doses given two weeks apart, followed by one dose every four weeks indefinitely. Each visit requires a lumbar puncture, which may cause temporary discomfort, headache, or back pain.

Lumbar Puncture Procedure
Tell patientEach dose requires a lumbar puncture. This involves a needle being inserted into the lower back to access the spinal fluid. It usually takes less than 30 minutes. Some back pain and headache are common afterwards — lying flat for 30–60 minutes and staying well hydrated can help reduce post-LP headache.
Call prescriberContact your care team if you develop severe headache that worsens when upright, persistent back pain, fever, or leg weakness after the procedure.
Serious Neurological Symptoms
Tell patientIn rare cases, tofersen can cause inflammation of the spinal cord (myelitis), nerve roots (radiculitis), or the lining of the brain (meningitis), as well as increased pressure inside the head. These are usually reversible with prompt treatment.
Call prescriberSeek immediate medical attention if you experience new or worsening weakness in arms or legs, numbness or tingling, vision changes, severe headache, neck stiffness, fever, or difficulty with bladder/bowel control.
Dosing Schedule
Tell patientTreatment starts with three doses given two weeks apart (loading phase), followed by one dose every four weeks (maintenance). Keeping to the schedule is important for maintaining drug levels in the spinal fluid. If you miss a dose, contact your care team promptly to reschedule.
Call prescriberIf you are unable to attend a scheduled dose or need to reschedule, notify the care team as soon as possible.
Accelerated Approval Status
Tell patientTofersen was approved based on its ability to lower a blood marker of nerve damage rather than a standard measure of daily function. Additional studies are ongoing to confirm the clinical benefit. This is common for treatments of rare diseases where waiting for full trial results would delay access to potentially beneficial therapy.
Call prescriberIf you have questions about the evidence supporting tofersen or want to discuss ongoing trial results, speak with your neurologist.
Pregnancy & Family Planning
Tell patientAnimal studies did not show harm to developing offspring at doses higher than the human dose. However, there are no studies in pregnant women. If you are of childbearing potential, discuss family planning with your care team.
Call prescriberNotify your doctor if you become pregnant, plan to become pregnant, or are considering breastfeeding.
Ref

Sources

Regulatory (PI / SmPC)
  1. Biogen MA Inc. QALSODY (tofersen) injection, for intrathecal use: US Prescribing Information. NDA 215887. Revised 04/2023. FDA LabelPrimary source for all dosing, pharmacokinetic, safety, and indication data in this monograph.
  2. US FDA. Approval letter and review documents for QALSODY (tofersen). NDA 215887. April 25, 2023. FDA Approval LetterRegulatory approval documentation under accelerated approval pathway; outlines postmarketing requirements including confirmatory trial.
Key Clinical Trials
  1. Miller TM, Cudkowicz ME, Genge A, et al. Trial of antisense oligonucleotide tofersen for SOD1 ALS. N Engl J Med. 2022;387(12):1099–1110. doi:10.1056/NEJMoa2204705Pivotal Phase 3 VALOR trial + OLE 12-month combined analysis. Primary endpoint (ALSFRS-R) not statistically significant; NfL reduction and SOD1 lowering achieved; early-start vs delayed-start analysis supported clinical benefit.
  2. Miller TM, Cudkowicz ME, Shaw PJ, et al. Phase 1–2 trial of antisense oligonucleotide tofersen for SOD1 ALS. N Engl J Med. 2020;383(2):109–119. doi:10.1056/NEJMoa2003715Dose-escalation Phase 1-2 study establishing safety, PK, and dose-dependent CSF SOD1 reduction; 100 mg dose selected for Phase 3.
  3. Miller TM, Cudkowicz ME, Shaw PJ, et al. Long-term tofersen in SOD1 amyotrophic lateral sclerosis. JAMA Neurol. Published online December 22, 2025. doi:10.1001/jamaneurol.2025.4946Final VALOR/OLE results over ~148 weeks (3.5 years) demonstrating sustained NfL reductions, numerically less functional decline with early-start tofersen, prolonged survival vs natural history, and ~25% of participants showing functional improvement.
  4. Benatar M, Wuu J, Andersen PM, et al. Design of a randomized, placebo-controlled, phase 3 trial of tofersen initiated in clinically presymptomatic SOD1 variant carriers: the ATLAS study. Neurotherapeutics. 2022;19(4):1248–1258. doi:10.1007/s13311-022-01286-7Design paper for the ATLAS confirmatory study evaluating tofersen in presymptomatic SOD1 carriers with elevated NfL; key for continued approval pathway.
Guidelines
  1. Miller RG, Jackson CE, Kasarskis EJ, et al. Practice parameter update: The care of the patient with amyotrophic lateral sclerosis: multidisciplinary care, symptom management, and cognitive/behavioral impairment. Neurology. 2009;73(15):1227–1233. doi:10.1212/WNL.0b013e3181bc01a4AAN guideline for ALS care; predates tofersen but provides the multidisciplinary framework within which genetically targeted ALS therapies are managed.
Mechanistic / Basic Science
  1. Rosen DR, Siddique T, Patterson D, et al. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature. 1993;362(6415):59–62. doi:10.1038/362059a0Landmark discovery of SOD1 mutations as a cause of familial ALS; foundational for the development of SOD1-targeted therapies including tofersen.
  2. Kiernan MC, Vucic S, Talbot K, et al. Improving clinical trial outcomes in amyotrophic lateral sclerosis. Nat Rev Neurol. 2021;17(2):104–118. doi:10.1038/s41582-020-00434-zComprehensive review of ALS trial design challenges, including discussion of biomarker-driven endpoints and genetic subtyping strategies relevant to tofersen’s approval pathway.
  3. Akcimen F, Lopez ER, Landers JE, et al. Amyotrophic lateral sclerosis: translating genetic discoveries into therapies. Nat Rev Genet. 2023;24(9):642–658. doi:10.1038/s41576-023-00592-yReview of genetic ALS therapies including ASOs; provides context for tofersen within the broader landscape of genetically targeted ALS drug development.
Pharmacokinetics / Special Populations
  1. Blair HA. Tofersen: first approval. Drugs. 2023;83(11):1039–1043. doi:10.1007/s40265-023-01904-6Concise drug approval summary covering pharmacology, clinical trial results, and regulatory context for tofersen.
  2. Benatar M, Wuu J, Andersen PM, Lombardi V, Malaspina A. Neurofilament light: a candidate biomarker of presymptomatic amyotrophic lateral sclerosis and phenoconversion. Ann Neurol. 2018;84(1):130–139. doi:10.1002/ana.25276Seminal Pre-fALS study demonstrating that serum NfL elevation precedes phenoconversion by ~12 months; foundational evidence for using NfL as a presymptomatic biomarker and informing the ATLAS trial design.