ALS Reversals - Lunasin Regimen
Ключови думи
Резюме
Описание
The primary hypothesis is that a supplement regimen containing Lunasin (referred to as the Lunasin regimen) can decrease the rate of ALSFRS-S progression by 50% relative to matched historic controls.
ALS is a devastating motor neuron disease that causes rapidly progressive muscle weakness, disability and premature death. In spite of a large number of attempted ALS trials, there are no significant disease-modifying therapies for this condition.
It was recently reported that a patient with a validated diagnosis of ALS, had experienced dramatic objective improvement in speech, swallowing and limb strength while taking a supplement regimen containing Lunasin. Several other patients with ALS have also reported improvement on this Lunasin regiment, though records were not obtainable to validate these.
The Lunasin regimen will consist of:
- LunaRich X Capsules
- Reliv NOW - a mixture of 'vitamins, minerals and super-powered antioxidants'
- Pro-Vantage - a mixture of 'soy protein, medium chain triglycerides, creatine, CoQ10 and supercharged amino acids'
Dosages will be titrated up to target over the first 6 days. The subject will take the highest tolerated dosing for the remainder of the 12-month study.
There are 3 in-clinic visits which occur at screening/baseline, Month 1 and Month 12. For Months 2-11, participants will make "virtual visits" by measuring their own ALSFRS-R score and weight and will record it in the PatientsLikeMe website. They will also self-report any perceived efficacy, compliance, adverse events and changes in concomitant medications.
Дати
| Последна проверка: | 10/31/2018 |
| Първо изпратено: | 03/04/2016 |
| Очаквано записване подадено: | 03/09/2016 |
| Първо публикувано: | 03/15/2016 |
| Изпратена последна актуализация: | 11/25/2018 |
| Последна актуализация публикувана: | 12/12/2018 |
| Дата на първите подадени резултати: | 07/24/2018 |
| Дата на първите подадени резултати от QC: | 11/25/2018 |
| Дата на първите публикувани резултати: | 12/12/2018 |
| Действителна начална дата на проучването: | 03/31/2016 |
| Приблизителна дата на първично завършване: | 09/12/2017 |
| Очаквана дата на завършване на проучването: | 09/12/2017 |
Състояние или заболяване
Интервенция / лечение
Drug: Lunasin regimen
Other: Historical controls
Фаза
Групи за ръце
| Arm | Интервенция / лечение |
|---|---|
| Experimental: Lunasin regimen The Lunasin regimen consists of:
LunaRich X Capsules (12 capsules per day)
Reliv NOW - a mixture of 'vitamins, minerals and super-powered antioxidants' (3 scoops per day)
Pro-Vantage - a mixture of 'soy protein, medium chain triglycerides, creatine, CoQ10 and supercharged amino acids' (2 scoops per day)
It will be suggested that patients open the LunaRich X capsules and mix the contents of these as well as the other 2 ingredients in water to make a shake. If patients do not tolerate advancing to the next dosage, they will be asked to drop back to the highest dosage they could tolerate. | Drug: Lunasin regimen LunaRich X Capsules, Reliv Now, ProVantage |
| Active Comparator: Historical controls For each enrolled participant, matched historical controls will be identified from the PatientsLikeMe database. Participants will be matched according to their ALSFRS-R progression rate before they start on the Lunasin regimen (estimated by assuming their score was normal at 48 on the date of symptom onset). | Other: Historical controls Matched historical controls will be identified from the PatientsLikeMe database. |
Критерии за допустимост
| Възрасти, отговарящи на условията за проучване | 18 Years Да се 18 Years |
| Полове, допустими за проучване | All |
| Приема здрави доброволци | Да |
| Критерии | Inclusion Criteria: - Male or female, aged at least 18 years. - Sporadic or familial ALS diagnosed as possible, laboratory-supported probable, probable, or definite as defined by revised El Escorial criteria. - Patient is able to understand and express informed consent (in the opinion of the site investigator). - Patient has access to the Internet on a desktop computer, laptop, or tablet and has a working email address. - Patient or caregiver is willing and able to use a computer and enter data on a secure website. - Patient is able to read and write English. - Women must not be able to become pregnant (e.g., post-menopausal, surgically sterile, or using adequate birth control methods) for the duration of the study and three months after study completion. Adequate contraception includes: abstinence, hormonal contraception (oral contraception, implanted contraception, injected contraception or other hormonal contraception, for example patch or contraceptive ring), intrauterine device (IUD) in place for ≥ 3 months, barrier method in conjunction with spermicide, or another adequate method. Exclusion Criteria: - Patient is taking other experimental treatments for ALS. - Prior side effects from Lunasin. - Known soy allergy. - Patient has a medical or psychiatric illness that could in the investigator's opinion interfere with the patient's ability to participate in this study. - Pregnant women or women currently breastfeeding. |
Резултат
Първични изходни мерки
1. Change in Revised ALS Functional Rating Scale (ALSFRS-R) [Screening/baseline - 12 months]
Вторични изходни мерки
1. Change in H3 Histone Acetylation [Screening/baseline, Month 1]
2. Percent Agreement Between the Weights Obtained by Patients and Study Coordinator [Month 1, Month 12]
3. Enrollment Rate [Screening/baseline - Month 12]
4. Retention Rate [Month 12]
5. Frequency of ALS Reversals [Screening/baseline - Month 12]
6. ALSFRS-R Accuracy [Month 1]
