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Chemotherapy Induced Peripheral Neuropathy (CIPN)Phase 3STING-CIPNNCT04715542

Stibium Metallicum Praeparatum D6 Versus Placebo in the Reduction of Paclitaxel-induced Peripheral Neurotoxicity

A Phase 3 study testing Stibium metallicum praeparatum 6x in people with Chemotherapy Induced Peripheral Neuropathy (CIPN), run by University of Bern.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

Chemotherapy induced peripheral neuropathy (CIPN) is one of the most limiting side effects of chemotherapy and often leads to adaptations in the protocol of the chemotherapy including dose reduction or even discontinuation of treatment. Read more about this study

Who is it for?
Ages 18 years and older, women only
What is being tested?
Stibium metallicum praeparatum 6x
Type of treatment
Injection or infusion
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
86 participants
Where
No sites listed yet
Study dates
Jan 2027to Dec 2029
Phase
Phase 3
Are there results?
Not yet: the study is under way

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 years and older
  • Women only
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age ≥ 18
  • Early breast cancer, ovarian cancer or other gynecological cancer
  • Patients who are about to receive a treatment with paclitaxel for 12 or 18 weeks (weekly or three-weekly) as part of adjuvant or neo-adjuvant chemotherapy.
  • Ability to provide informed consent as documented by signature
  • Ability to read, write, and speak German

Who cannot join

  • Patients with pre-existing neuropathy
  • Prior chemotherapy with taxanes or other neurotoxic agents
  • Concomitant medications that are known to cause neuropathy
  • Pregnancy or lactation
  • Lack of safe contraception, defined as: female participants of childbearing potential, not using and not willing to continue using a medically reliable method of contraception for the entire study duration, such as oral, injectable, or implantable contraceptives, or intrauterine contraceptive devices, or who are not using any other method considered sufficiently reliable by the investigator in individual cases.
  • Patients with depression or epilepsy
  • Allergy to milk protein

Trial locations and contacts

No sites are listed yet. Contact the study team or a site near you to ask about taking part.

Silvia Erni, PhD contact

+41316841563

silvia.erni@unibe.ch

About this study

Official title: A Randomized, Double-blind, Placebo-controlled Multicenter Study Evaluating Stibium Metallicum Praeparatum D6 for Reducing Chemotherapy-induced Peripheral Neuropathy in Breast and Gynecological Cancer Patients Receiving Paclitaxel

Chemotherapy induced peripheral neuropathy (CIPN) is one of the most limiting side effects of chemotherapy and often leads to adaptations in the protocol of the chemotherapy including dose reduction or even discontinuation of treatment. In general, the symptoms of CIPN are sensory, often distributed in a "stocking and glove" manner, and include pain, tingling, and numbness. CIPN has a marked negative influence on quality of life of patients and their families. It may result in serious limitations in daily functioning and affect the enjoyment, social relationships, and ability to perform work. Current management of CIPN (i.e. prevention and treatment) includes dose reduction or delay of chemotherapy cycles and treatment discontinuation. Unfortunately, this reduces the chance of an effective cancer treatment. Current guidelines of the American Society of Clinical Oncology (ASCO) on the Prevention and Management of Chemotherapy-Induced Peripheral Neuropathy do not conclusively recommend any agent for the prevention of CIPN. Due to the scarcity of drugs that are effective for preventing and treating CIPN, the distress of patients who suffer from CIPN, and the major societal and economic costs, new approaches and effective treatment strategies are required.

The proposed trial is a parallel, double blind, placebo controlled, randomised trial, aiming to determine whether treatment with SMP reduces the severity of symptoms of paclitaxel-induced peripheral neuropathy, as compared to placebo.

Read the detailed description

Chemotherapy-induced peripheral neuropathy (CIPN) is one of the most limiting side effects of chemotherapy and often leads to adaptations in the administration of the chemotherapy, including dose reduction or even discontinuation of treatment. In general, the symptoms of CIPN are sensory, often occuring in a "stocking and glove" manner, and most commonly including tingling, numbness, and dysaesthesia. In addition, patients treated with agents inducing CIPN, such as taxanes or platinum compounds, also may experience motor symptoms, which often present as distal or general weakness, and autonomic nervous system dysfunction (e.g. constipation or diarrhea, abnormalities of sweating, and lightheadedness and/or dizziness with positional changes). Furthermore, patients with chronic symptoms report having unsteady gait, putting them at higher risk of falling. CIPN has a largest impact on quality of life and is associated with the development of psychological distress. Cancer survivors' report long-term peripheral neuropathy symptoms with impact on symptom burden, functional status, and quality of life. Because of the growing prevalence of cancer and of cancer survivors, the lack of adequate treatment or preventive strategies against CIPN, as well as the major societal and economic costs, CIPN is becoming a major issue.

According to the National Comprehensive Cancer Network (NCCN) task force report, the overall incidence of CIPN ranges from 57 up to 83% of patients treated with paclitaxel. The incidence and prevalence of CIPN vary among neurotoxic agents, dosing regimens (intensity and cumulative dosing), regimen selection (e.g. combination taxanes and platinum compounds), as well as in presence of preexisting neuropathy, comorbidities and genetic susceptibility. The analysis of the Japanese Adverse Drug Event Report database showed that more than 50% of CIPN associated with taxanes and platinum compounds occurred within four weeks.

After completion of chemotherapy, the prevalence of CIPN for neurotoxic chemotherapy overall one month after finishing chemotherapy is 68%, dropping to 60% at 3 months and 30% at 6 months or more. Severe symptoms are likely to persist longer. In patients treated with taxanes, nearly half of patients have symptoms 6 to 9 months after completing chemotherapy, and many require years to recover, if they recover at all. In early-stage breast cancer patients treated with paclitaxel, persistent numbness one year after treatment with paclitaxel were reported in approximately 67% to 80% of early-stage breast cancer patients. Two years after the end of therapy, 34.4% of breast cancer patients treated with paclitaxel reported neuropathy symptoms, with 18.0% reporting more severe symptoms. Another study showed that two or more years after diagnosis, 44% of breast cancer survivors treated with paclitaxel reported long-term neuropathy symptoms.

Current management of CIPN (i.e. prevention and treatment) includes dose reduction, delay of chemotherapy cycles, or treatment discontinuation. This reduces the chance of an effective cancer treatment.

The 2014, 2020, and 2021 American Society of Clinical Oncology (ASCO) Guidelines on the Prevention and Management of Chemotherapy-Induced Peripheral Neuropathy did not recommend any agent for the prevention of CIPN, and have cautiously recommended treatment of existing CIPN with duloxetine. Preliminary evidence suggests a potential benefit from non-pharmacological treatments in the prevention and/or treatment of chronic neuropathy including exercise, acupuncture, cryotherapy, compression therapy, and scrambler therapy. Larger sample-sized definitive studies are needed to confirm efficacy and clarify risks of these interventions.

Cumulative dose is a strong risk factor for the development of CIPN. Other risk factors include dose per cycle, treatment schedule (number of injections), duration of infusion, prior or concomitant chemotherapy with neurotoxic agents (i.e. vinca alkaloids, taxanes, platinum compounds, epothilones including ixabepilone, bortezomib, thalidomide, arsenice trioxides), development and severity of acute neuropathy syndrome or acute pain syndrome within 1 to 4 days following the neurotoxic agent infusion, comorbid health conditions associated with an increased risk of neuropathy (i.e. diabetes mellitus, excess alcohol, HIV, smoking, decreased creatinine clearance, folate/vitamin B12 deficiency), pre-existing peripheral neuropathy, older age, and higher body mass index. Other clinical risk factors such as sedentary behavior, insomnia, fatigue, anxiety, and depression have been shown to increase CIPN prevalence. Genetic factors may also be associated with risk of developing CIPN.

Due to the scarcity of drugs that are effective for preventing and treating CIPN, the distress of patients who suffer from CIPN, and the major societal and economic costs, new approaches and effective treatment strategies are required. This study investigates the efficacy and tolerance of Stibium metallicum praeparatum D6 (Weleda), also known as Antimon, to reduce paclitaxel-induced peripheral neuropathy as reported by patients. As secondary outcomes, the influence on quality of life as well as on chemotherapy treatment adherence and dose of chemotherapy delivered is assessed.

Being tested
Stibium metallicum praeparatum 6x, Placebo

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Stibium metallicum praeparatum 6xDrug

    Stibium metallicum praeparatum D6 will be administered with subcutaneous injections 3 times a week at 1 ampoule at 1 mL during the chemotherapy and shall be continued during 6 weeks after the end of chemotherapy . The first injection will be administered on the day of the first dose of chemotherapy, before the injection of the first dose of chemotherapy.

  • PlaceboDrug

    Placebo will be administered with subcutaneous injections 3 times a week at 1 ampoule at 1 mL during the chemotherapy and shall be continued during 6 weeks after the end of chemotherapy . The first injection will be administered on the day of the first dose of chemotherapy, before the injection of the first dose of chemotherapy.

Study groups in NCT04715542
Study groupRoleWhat they receive
Stibium metallicum praeparatum D6ExperimentalPatients are treated with Stibium metallicum praeparatum D6 (subcutaneus injection), which is authorized in Switzerland and is listed by Swissmedic as an authorized anthroposophic medicinal product.
Receives: Drug: Stibium metallicum praeparatum 6x
Saline subcutaneous injectionPlacebo comparatorPlacebo (a saline subcutaneous injection) is chosen as comparator to the treatment group.
Receives: Drug: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Reduction in neuropathy severity

    Measured by the neurotoxicity subscale (NTX-subscale) of the FACT/GOG-NTX questionnaire (FACT/GOG-NTX: Functional Assessment of Cancer Therapy/Gynecologic Oncology Group-Neurotoxicity, Score rage of NTX-subscale: 0-44, the higher the score, the better the QOL)

    Measured: Weekly from week 1 (Baseline) - 13

Secondary outcomes (5)
  1. Occurrence and severity of paclitaxel-induced peripheral neuropathy over the whole study period

    Measured by the NTX-subscale of the FACT/GOG-NTX questionnaire

    Measured: 12-week chemotherapy: Weekly from week 1-19 and week 24, 36, 48, 60; 18-week chemotherapy: Weekly from week 1-25, and week 30, 42, 54, 66

  2. Oncologist's evaluation CIPN

    Assessed by oncologist using the CTCAE grading system

    Measured: 12-week chemotherapy: Week 1, 4, 7, 10, 13, 19, 24, 36, 48, 60; 18-week chemotherapy: Week 1, 4, 7, 10, 13, 16, 19, 25, 30, 42, 54, 66

  3. Chemotherapy adherence

    Record whether all chemotherapy cycles could be administered as planned (indicate chemotherapy interruptions, dose reductions and discontinuations)

    Measured: 12-week chemotherapy: Week 13; 18-week chemotherapy: Week 19

  4. Effect on Quality of life (QOL)

    Assessed by the FACT-G questionnaire (FACT-G: Functional Assessment of Cancer Therapy - General, Score range: 0-108, the higher the score, the better the QOL)

    Measured: 12-week chemotherapy: Week 1, 7, 13, 19, 24, 36, 48, 60; 18-week chemotherapy: Week 1, 7, 13, 19, 25, 30, 42, 54, 60

  5. Biomarker for CIPN

    Detection of Neurofilament light chain (NfL) and Glial Fibrillary Acidic Protein (GFAP) levels in blood serum

    Measured: Week 1, 13, 19

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted20 Jan 2021
  2. Study startJan 2027 (estimated)
  3. Primary completionJan 2029 (estimated)
  4. Study completionDec 2029 (estimated)

Resources

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 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
Randomized-controlled, double-blind, multicentric trial
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
86 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04715542
Sponsor's protocol ID
12012021
Acronym
STING-CIPN
Status last verified
Sep 2026
First submitted
14 Jan 2021
Last updated
15 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: IPD will never be available to other researchers who are not part of the core research group. Unblinding is explicitly not foreseen for this study. Maintaining blinding until all participants complete the study protocol, the data base is locked and analysis is completed, will help retain trial integrity of this double-blinded study.

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Stibium metallicum praeparatum 6x in people with Chemotherapy Induced Peripheral Neuropathy (CIPN), run by University of Bern.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 15 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Silvia Erni, PhD (+41316841563, silvia.erni@unibe.ch), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Reduction in neuropathy severity (time frame: Weekly from week 1 (Baseline) - 13). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 15 Sep 2026.

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