Breast CancerPhase 2NCT07889115
Evaluation of the Effect of Amantadine in the Prevention of Paclitaxel-Induced Peripheral Neuropathy in Breast Cancer Patients
A Phase 2 study testing Amantadine (oral) in people with Breast Cancer and Peripheral Neuropathy Due to Chemotherapy, run by Al-Azhar University.
Trial summary
This randomized, controlled, open-label trial will evaluate the efficacy and safety of amantadine, an NMDA receptor antagonist with antioxidant and anti-inflammatory properties, in preventing paclitaxel-induced peripheral neuropathy (PIPN) in breast cancer patients receiving weekly paclitaxel. Read more about this study
- Who is it for?
- Ages 18 to 65 years, women only
- Conditions the study is for
- Breast Cancer, Peripheral Neuropathy Due to Chemotherapy, VAS Score
- What is being tested?
- Amantadine (oral)
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 80 participants
- Where
- No sites listed yet
- Study dates
- 1 Dec 2026to 1 Jan 2028
- Phase
- Phase 2
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- Women only
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Adult patients (>18 years old).
- Patients with confirmed diagnosis of non-metastatic breast cancer planned to receive weekly adjuvant/neo-adjuvant paclitaxel.
- Patients with Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
Who cannot join
- Patients with pre-existing neuropathic conditions.
- Patients with diabetes mellitus.
- Patients with a history of seizure disorder.
- Patients with renal impairment (creatinine clearance less than 60 ml/min), or hepatic impairment (defined as ALT an AST > 3 times upper limits of normal)
- Patients with inadequate bone marrow functions (defined as absolute neutrophilic count less than 1,500/mm³ or platelets count less than 100,000/mm³).
- Concomitant use of vitamin B1, B6, B9, or B12.
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- Patients receiving medications that possibly induce peripheral neuropathy including amiodarone, colchicine, metronidazole, antimycobacterials, and nucleoside reverse transcriptase inhibitors, and phenytoin (Jones et al., 2020).
- Patients receiving gabapentinoids, antidepressants, or opioids.
- Pregnancy or lactation.
- History of hypersensitivity to amantadine
- Concurrent use of anticholinergic drugs (e.g., antihistamines, tricyclic antidepressants, antipsychotics, antispasmodics, or antiparkinsonian agents) within 2 weeks before enrollment, except for short-term use of antiemetics prescribed as part of standard chemotherapy supportive care (e.g., prochlorperazine, promethazine).
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Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
This randomized, controlled, open-label trial will evaluate the efficacy and safety of amantadine, an NMDA receptor antagonist with antioxidant and anti-inflammatory properties, in preventing paclitaxel-induced peripheral neuropathy (PIPN) in breast cancer patients receiving weekly paclitaxel.
Read the detailed description
Cancer persists as a predominant contributor to global morbidity and mortality (DeSantis et al., 2016) . Despite the established cytotoxic efficacy of chemotherapeutic agents in impeding tumor progression through the eradication of highly proliferative malignant cells, their clinical utility is frequently constrained by deleterious systemic toxicities. Among these, chemotherapy-induced peripheral neuropathy (CIPN) constitutes a severe, dose-limiting clinical toxicity associated with specific chemotherapeutic regimens (Zhang et al., 2017) . For a substantial proportion of patients, CIPN manifests as profoundly debilitating symptoms that compromise functional independence and activities of daily living (ADL), alongside a significant deterioration in health-related quality of life (QoL). Such clinical deterioration often mandates therapeutic dose attenuation and/or treatment delays, leading to suboptimal oncological outcomes and the prolongation of therapeutic cycles.(Smith et al., 2013a)
This neurotoxicity is strongly associated with specific classes of cytotoxic agents, including taxanes, platinum-based compounds, and vinca alkaloids, as well as immunomodulatory agents such as thalidomide and lenalidomide, and the proteasome inhibitor bortezomib (Kottschade et al., 2011) . Although prospective identification of patients predisposed to CIPN presents a significant clinical challenge, established risk factors encompass antecedent exposure to neurotoxic agents, diabetes mellitus, folate or vitamin B12 deficiencies, African ethnicity, and advanced age (Brewer et al., 2016) .
Paclitaxel represents a first-line chemotherapeutic modality for solid tumors. Its principal antineoplastic mechanism involves the disruption of mitotic spindle assembly and microtubule dynamics, ultimately triggering apoptotic cell death. Nevertheless, the major dose-limiting toxicity associated with its clinical use is dose-dependent sensory peripheral neuropathy )(Duggett et al., 2016; Scripture et al., 2006) .
The incidence of paclitaxel-induced peripheral neuropathy (PIPN) can reach up to 97% among treated patients, with a chronic course observed in more than 60% of cases (Tanabe et al., 2013) . The initial clinical manifestations of PIPN encompass paresthesia (numbness and tingling) and/or allodynia, defined as painful sensations elicited by normally non-noxious stimuli-which may develop in the patient's fingers and toes within 24 to 72 hours post-injection. These sensory symptoms may subsequently progress to involve the lower legs and wrists in a characteristic "glove and stocking" distribution. Typically, symptoms initiate distally and advance proximally in tandem with clinical deterioration (Argyriou et al., 2008; Smith et al., 2013b) .
The pathogenesis of paclitaxel-induced peripheral neuropathy is multifactorial, primarily driven by the generation of reactive oxygen species (ROS)-including superoxide, hydroxyl radicals, nitric oxide, and hydrogen peroxide-within neuronal mitochondria. This oxidative stress is accompanied by the elaboration of pro-inflammatory cytokines, such as interleukin-1 beta (IL-1β), tumor necrosis factor-alpha (TNF-α), and interleukin-6 (IL-6), largely secondary to the activation of microglia and astrocytes, alongside other interconnected mechanisms (Carvalho et al., 2017; Sisignano et al., 2014) .
Glutamate serves as the principal excitatory neurotransmitter, orchestrating essential physiological processes such as learning and memory. Elevated concentrations of glutamate are implicated in excitotoxic cascades that culminate in neuronal death (Willard \& Koochekpour, 2013) . In rodent models treated with paclitaxel, the baseline frequency of excitatory postsynaptic currents was significantly elevated; notably, N-methyl-D-aspartate (NMDA) receptor antagonists completely normalized this aberrant frequency (Xie et al., 2016) . Furthermore, NMDA receptor signaling and glutamatergic pathways have been strongly implicated in the genesis of neuronal hyperexcitability. Consequently, the authors posited a pivotal therapeutic role for NMDA receptor antagonism in mitigating taxane-induced neuropathy (Drummond et al., 2024) . Correspondingly, Mihara et al. Delineated the involvement of NMDA receptors in the pathophysiology of oxaliplatin-induced mechanical allodynia in rodent models (Mihara et al., 2011) . The NMDA receptor is an ionotropic channel integral to mediating glutamatergic neurotransmission. Excessive activity of this receptor is pathogenically linked to spasticity alongside acute pain manifestations, which, if left untreated or if the ongoing insult persists, invariably progress to chronic neuropathic pain. Concurrently, NMDA receptor activation facilitates the release of substance P within the dorsal horn, thereby propagating central sensitization through synaptic remodeling. This process is further potentiated by augmented glutamate release via presynaptic NMDA receptors (Pușcașu et al., 2024) .
Considering the complex and multifactorial nature of PIPN, an ideal therapeutic intervention would need to address both its central and peripheral components. The central mechanism is characterized by NMDA receptor-driven hyperexcitability, which preclinical studies have demonstrated can be attenuated by NMDA antagonists (Xie et al., 2016). In parallel, the peripheral mechanism is primarily mediated by oxidative stress and neuroinflammation, evidenced by the accumulation of reactive oxygen species (ROS) and pro-inflammatory cytokines, including TNF-α and IL-6 (Sisignano et al., 2014; Carvalho et al., 2017). Therefore, a drug that combines NMDA receptor antagonism with antioxidant and anti-inflammatory actions may provide a more comprehensive neuroprotective strategy. Amantadine, a non-competitive NMDA receptor antagonist that also possesses antioxidant and anti-inflammatory properties, emerges as a rational candidate for such a dual-action approach. Nevertheless, its role in preventing PIPN has not yet been investigated.
To date, no approved therapeutic interventions exist for the prevention of PIPN. Although numerous agents have been investigated for the management of CIPN, duloxetine remains the only therapeutic option with established clinical efficacy. Consequently, further research is imperative to develop both preventive and ameliorative strategies for PIPN (Jordan et al., 2020; Loprinzi et al., 2020) .
Amantadine is a non-competitive NMDA receptor antagonist that mitigates neuronal excitotoxicity by attenuating the prolonged influx of calcium ions, while preserving physiological NMDA receptor function (Blanpied et al., 2005) . Beyond its central action, amantadine has demonstrated significant antioxidant and anti-inflammatory properties in preclinical models. Specifically, it elevated glutathione (GSH) levels and reduced lipid peroxidation (LP), alongside downregulating pro-inflammatory cytokines such as TNF-α and IL-6 in a vincristine-induced peripheral neuropathy model (Drummond et al., 2024) . This dual mechanism-central NMDA receptor antagonism coupled with peripheral antioxidant and anti-inflammatory neuroprotection-positions amantadine as a rationally targeted and promising candidate for the prevention of PIPN, a condition in which both pathways are critically implicated.
The therapeutic potential of amantadine in neuropathic pain has been supported by both clinical and preclinical investigations. Clinically, a double-blind, randomized, placebo-controlled trial demonstrated that intravenous amantadine infusion produced an average pain reduction of 85% in cancer patients with surgical neuropathic pain, compared with 45% following placebo administration, establishing it as a safe and effective acute treatment (Pud et al., 1998) . Similarly, a pilot study in patients with painful diabetic peripheral neuropathy showed that intravenous amantadine provided sustained pain relief for at least one week post-infusion (Amin \& Sturrock, 2003) . Preclinically, amantadine has demonstrated antinociceptive, anti-inflammatory, and antioxidant effects in a vincristine-induced peripheral neuropathy model in rats (Drummond et al., 2024) . Mechanistically, amantadine treatment significantly decreased lipid peroxidation (LP) and increased glutathione (GSH) levels in injured neural tissue, effects mediated through NMDA receptor antagonism (Mata-Bermudez et al., 2021). These dual findings-clinical analgesic efficacy and preclinical neuroprotective mechanisms-provide a strong rationale for investigating amantadine as a preventive strategy for PIPN.
- Being tested
- Amantadine (oral)
- Keywords
- Breast cancer, Peripheral neuropathy, Paclitaxel- induced peripheral neuropathy, Amantadine, FACT/GOG-Ntx, VAS, Serum NGF, NCI-CTCAE
- Medical subject headings
- Breast Neoplasms, Peripheral Nervous System Diseases
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Amantadine (oral)Drug
Amantadine will be given orally at 100 mg once daily (100 mg arm) or 100 mg twice daily, 200 mg/day total (200 mg arm). It starts 3 days before the first paclitaxel dose and continues for 12 weeks, in addition to standard weekly paclitaxel (80 mg/m²).
| Study group | Role | What they receive |
|---|---|---|
| Amantadine100mg+paclitaxel 80 mg/m² weekly | Experimental | Amantadine 100 mg: amantadine 100 mg orally once daily, starting 3 days before the first paclitaxel dose, for 12 weeks, plus paclitaxel 80 mg/m² weekly. Receives: Drug: Amantadine (oral) |
| Amantadine 200mg+ paclitaxel 80 mg/m² weekly. | Experimental | Amantadine 200 mg: amantadine 100 mg orally twice daily (200 mg/day), same timing and duration, plus paclitaxel 80 mg/m² weekly. Receives: Drug: Amantadine (oral) |
| Control | Active comparator | paclitaxel 80 mg/m² weekly alone for 12 weeks. Receives: Drug: Amantadine (oral) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Incidence and severity of PIPN
All enrolled patients will receive education regarding the clinical manifestations of PIPN and will be encouraged to report any emerging symptoms. Additionally, a comprehensive neurological assessment will be conducted every cycle to evaluate the presence and severity of PIPN. The severity of PIPN will be graded according to the National Cancer Institute's Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 5, published in November 2017 (NCI, 2017).
The NCI-CTCAE classifies adverse events on a 5-point severity scale, as summarized in Table 1.
Table 1. NCI-CTCAE v5.0 Grading Scale for Peripheral Neuropathy
Grade
Description
Grade 1
Mild or asymptomatic symptoms necessitating clinical or diagnostic observation only; no intervention required.
Grade 2
Moderate symptoms that limit age-appropriate activities of daily living (ADL); minimal, local, or noninvasive intervention is indicated.
Grade 3
Severe or medically significant but not life-threatening symptoms th
Measured: Weekly from base line to week 12
Secondary outcomes (4)
Time to Neuropathy
Time to neuropathy is defined as the interval from the initiation of paclitaxel therapy (first dose) to the first occurrence of Grade ≥ 2 PIPN, as determined by the NCI-CTCAE v5.0 criteria. This outcome reflects the duration for which the patient remains free from clinically significant neuropathy.
Patients who do not develop Grade ≥ 2 PIPN by the end of the 12-week treatment period, or who withdraw from the study before developing this endpoint, will be censored at their last assessment visit.
Measured: Weekly from base line to week12
Change in Pain Intensity (vas)
Pain intensity will be assessed using the Visual Analogue Scale (VAS), a unidimensional measure of pain intensity originally validated by Huskisson (1974). The VAS consists of a 100-mm horizontal line, where the left end represents "no pain" (0 mm) and the right end represents "worst imaginable pain" (100 mm). Patients will be asked to mark the point on the line that best reflects their current level of pain. The score is determined by measuring the distance in millimeters from the left anchor to the patient's mark.
Figure 1. Visual Analogue Scale (VAS) for Pain Assessment
No pain Worst imaginable pain
0 mm 100 mm
The VAS will be administered at baseline and weekly during the 12-week treatment period. The change in VAS score from baseline to Week 12 will be calculated for each patient, with a reduction in score indicating an improvement in pain intensity
Measured: Weekly from base line to week 12
Change in Patient Quality of Life
Patients' QoL will be assessed through The Functional Assessment of Cancer Therapy/Gynecologic Oncology Group-Neurotoxicity subscale (FACT/GOG-Ntx) questionnaire. The Ntx subscale is a reliable and valid instrument for assessing the impact of neuropathy on QoL that demonstrates sensitivity to meaningful clinical distinctions and change over time (Calhoun et al., 2003) .
It is an eleven-item subscale that evaluates sensory neuropathy, motor neuropathy, hearing neuropathy, and dysfunction associated with CIPN for the previous 7 days. Each question in the Ntx subscale is represented by a Likert scale ranging from zero to four, where zero represents "not at all" and four represents "very much". The Ntx subscale generates a total score that is obtained by summation of the composing questions' scores. The total score ranges from 0 to 44 with higher scores indicating more severe neurotoxicity and worse QoL (HUANG et al., 2007) . The FACT/GOG-Ntx subscale will be evaluated at baseline, Week
Measured: at Base line,week6,week12
Change in serum NGF level
Nerve growth factor (NGF), one of the major neurotrophins, is known to regulate the growth, maintenance, and survival of neurons, and its signalling interacts closely with glutamatergic N-methyl-D-aspartate (NMDA) receptor pathways. Clinical evidence supports that depletion of NGF occurs during the development of CIPN. In cancer patients receiving taxanes, serum levels of NGF were shown to decrease after four to six cycles, and this decline was associated with the severity of PIPN (Rodwin et al., 2022; Youk et al., 2017) . Given that paclitaxel-induced NMDA receptor hyperactivation contributes to excitotoxicity and neurotrophic dysregulation, the NMDA-antagonistic effect of amantadine may help preserve endogenous NGF levels, thereby mitigating neurotoxicity.
For determination of serum levels of NGF, a blood sample of 4 ml will be collected from every patient at baseline and at Week 12 (end of paclitaxel treatment) by means of a venous puncture and will be placed in gel vacutainer tub
Measured: At base line and week12
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Oct 2026
- Study start1 Dec 2026 (estimated)
- Primary completion1 Dec 2027 (estimated)
- Study completion1 Jan 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Breast CancerStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 80 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Al-Azhar University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Amina Abdel Latif Mohamed El-Basyouni, Al-Azhar University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07889115
- Sponsor's protocol ID
- PIPN
- Status last verified
- Oct 2026
- First submitted
- 16 Oct 2026
- Last updated
- 22 Oct 2026
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided