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Not yet recruitingNCT04715542STING-CIPNUpdated Sep 15, 2026

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

A Phase 3 interventional study of Stibium metallicum praeparatum 6x and Placebo in Chemotherapy Induced Peripheral Neuropathy (CIPN), sponsored by University of Bern. Not yet recruiting. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-15.

Sponsored by University of Bern · Phase 3, Interventional, and Treatment

Phase
Phase 3
Study type
Interventional
Enrollment
86
Allocation
Randomized
Ages
18 Years and older
Sex
Female
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Study 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. 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.

02

Conditions studied

  • Chemotherapy Induced Peripheral Neuropathy (CIPN)
03

In context

Lead sponsor

University of Bern is the lead sponsor of 209 studies on the registry; 47 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 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 or neo-adjuvant chemotherapy.
  • Ability to provide as documented by signature
  • Ability to read, write, and speak German

Exclusion criteria

Exclusion Criteria:

  • 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 , defined as: female participants of , 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
Terms in these criteria, in plain language(4)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Adjuvant and neoadjuvant

Neoadjuvant treatment is given before the main treatment (usually surgery), often to shrink a tumour. Adjuvant treatment is given after it, to lower the chance of the cancer coming back.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
86 participants (estimated)

Study arms

  • Experimental
    Stibium metallicum praeparatum D6

    Patients 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.

    Drug: Stibium metallicum praeparatum 6x

  • Placebo comparator
    Saline subcutaneous injection

    Placebo (a saline subcutaneous injection) is chosen as comparator to the treatment group.

    Drug: Placebo

Interventions

  • DrugStibium metallicum praeparatum 6x

    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.

  • DrugPlacebo

    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.

06

What researchers measure

Primary outcomes

  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)

    Time frame: Weekly from week 1 (Baseline) - 13

Secondary outcomes

  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

    Time frame: 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

    Time frame: 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)

    Time frame: 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)

    Time frame: 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

    Time frame: Week 1, 13, 19

Other outcomes

  1. Adherence to study medication (I)

    Assessed by self-report

    Time frame: 12-week chemotherapy: Weekly from week 1-19; 18-week chemotherapy: Weekly from week 1-25

  2. Adherence to study medication (II)

    Assessed by returned unused medication

    Time frame: 12-week chemotherapy: Week 19; 18-week chemotherapy: Week 25

  3. Severe adverse events

    Recorded incidence and severity of adverse events

    Time frame: 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

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: 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.

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Jan 2027; primary completion for Jan 2029, 24 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Jan 14, 2021
First posted
Jan 20, 2021
StartEst.
Jan 2027
Primary completionEst.
Jan 2029
CompletionEst.
Dec 2029
Last update
Sep 15, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 15, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04715542
Lead sponsor
University of Bern
Responsible party
Sponsor
First posted
Jan 20, 2021
Start date
Jan 2027 (estimated)
Primary completion
Jan 2029 (estimated)
Completion
Dec 2029 (estimated)
Last update
Sep 15, 2026

Study contacts

Silvia Erni, PhD
Contact
silvia.erni@unibe.ch
+41316841563
Ursula Wolf, Prof. Dr.
study director · University of Bern
Anton Oseledchyk, PD Dr. med.
principal investigator · University Hospital, Basel, Switzerland

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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