Casperome® (Boswellia Phytosome — Indena)

Boswellia serrata
Evidence Level
Limited
5 Clinical Trials
4 Documented Benefits
2/5 Evidence Score

Casperome® is Indena's Boswellia serrata gum resin extract bound to lecithin in a Phytosome® form, standardized to at least 25% triterpenoid acids. Boswellic acids are poorly absorbed from ordinary boswellia extracts, and the lecithin form was built to fix that: in a small crossover study in 12 healthy volunteers, most boswellic acids reached higher and faster blood levels than from the same dose of plain extract. Human studies of effects are still early. For sports knee pain and ankle sprains, the evidence comes from open-label registry studies in which people chose their own group, so placebo effects cannot be ruled out. The one double-blind, placebo-controlled trial found so far tested short-term diarrhea, not joints. Most studies were run or funded by Indena.

Studied Dose 250 mg once daily for 7 days in the ankle sprain registry study; one tablet daily for 6 months in an IBS study; 250 mg twice daily for 5 days in the diarrhea trial; 2 x 250 mg as a single dose in the absorption study.
Active Compound Boswellia serrata gum resin extract formulated with lecithin (Phytosome®), standardized to at least 25% triterpenoid acids. Early papers describe soy lecithin; a 2022 trial used a sunflower lecithin version.

Benefits

Better absorption of boswellic acids

In a randomized, open-label crossover study in 12 healthy volunteers given 2 x 250 mg, the lecithin form produced significantly higher and faster blood levels of most boswellic acids than the same dose of plain extract; KBA was the exception. Better absorption has not yet been shown to give better results than plain boswellia in people.

Joint comfort and inflammation markers after sports strains

In open-label registry studies, 25 young rugby players with knee pain and 35 adults with grade II ankle sprains who chose Casperome alongside standard care reported less pain and needed fewer rescue pain relievers than those on standard care alone. Inflammation markers also fell in the rugby study. People picked their own group and there was no placebo, so this evidence is preliminary.

Faster return to normal bowel habits

In a double-blind, placebo-controlled trial in 49 adults with short-term diarrhea, 250 mg twice daily for 5 days shortened the time to recovery (about 3.1 vs 4.4 days) and reduced stool frequency, belly pain and nausea. This is a single small trial co-authored by Indena staff.

Digestive comfort: bloating, cramps and bowel habits

In a 6-month study of 69 adults with mild IBS, people taking one Casperome tablet daily had lower scores for most symptoms and needed fewer rescue medicines and medical visits than people on standard antispasmodic care. In a 4-week study of 71 adults, symptoms improved in all groups, with fewer medical visits on Casperome. Neither study used a placebo, so the results are preliminary.

Mechanism of action

1

Lecithin delivery form

Binding the extract to lecithin helps the poorly water-soluble boswellic acids cross the gut wall. In mice, the lecithin form gave up to 7-fold higher blood levels of KBA and 3-fold higher levels of β-boswellic acid than plain extract, with higher tissue levels as well.

2

Prostaglandin and leukotriene pathways

Boswellic acids were long thought to work by blocking 5-lipoxygenase, which makes leukotrienes. A pharmacology review noted that blood levels of AKBA after oral boswellia are too low for that to be certain and pointed to β-boswellic acid acting on microsomal prostaglandin E synthase-1 and cathepsin G instead. These are lab findings.

Clinical trials

1
Casperome Absorption Crossover Study
PubMed

Single-dose, randomized, open-label, two-way crossover study comparing Casperome with the same plain Boswellia serrata extract at 2 x 250 mg. (Riva et al. 2016, Phytomedicine)

12 healthy volunteers.

Except for KBA, boswellic acids were absorbed significantly more and faster from Casperome, both by weight and by molar dose, reaching peak levels in the range needed to act on their lab targets. Co-authored by Indena staff.

2
Casperome for Knee Pain in Young Rugby Players
PubMed

Open-label registry study over 4 weeks; participants chose standard management alone or with daily Casperome. (Franceschi et al. 2016, Eur Rev Med Pharmacol Sci)

52 healthy young rugby players with acute knee pain (25 Casperome, 27 control).

The Casperome group did better on effort pain, pain-free walking distance, joint swelling, VAS pain, need for other drugs and inflammatory blood markers. There was no placebo or blinding and groups were self-selected.

3
Casperome for Grade II Ankle Sprains
PubMed

Open-label supplement registry study over 7 days; participants chose standard management alone or with 250 mg Casperome daily, with ketoprofen allowed as rescue medication. (Feragalli et al. 2017, Eur Rev Med Pharmacol Sci)

72 otherwise healthy adults with sports-related grade II ankle sprains (35 Casperome, 37 control).

Signs and symptoms improved more with Casperome at days 3 and 7, rescue drug use was lower, and boswellic acids were measurable in blood. No side effects were reported. Self-selected groups without placebo; the authors called it a pilot study.

4
Casperome for Short-Term Diarrhea
PubMed

Randomized, double-blind, placebo-controlled trial of 250 mg Casperome twice daily for 5 days. (Giacosa et al. 2022, Nutrients)

49 adults with acute diarrhea.

Time to recovery was shorter with Casperome (3.08 vs 4.44 days), with fewer stools and less abdominal pain and nausea than placebo. Three authors are Indena employees.

5
Casperome for Mild IBS Over 6 Months
PubMed

Randomized comparison of one Casperome tablet daily versus standard management (diet plus antispasmodic drugs as needed), with no placebo. (Riva et al. 2019, Minerva Gastroenterol Dietol)

69 otherwise healthy adults with mild IBS.

The Casperome group had lower scores for most self-rated IBS symptoms, needed fewer rescue medications and medical visits, and had fewer minor side effects such as constipation than the standard-care group.

Side effects and drug interactions

Common Potential side effects

No relevant side effects were reported in the Casperome studies, which lasted from 5 days to 6 months.
In the IBS studies, minor side effects such as constipation were less common with Casperome than with antispasmodic drugs.
The lecithin in Casperome has been soy-based in some versions; people with a soy allergy should check the product label.

Important Drug interactions

Pain relievers (NSAIDs): Casperome has not been formally tested with NSAIDs; ask your doctor before combining them.
Blood thinners and antiplatelet drugs: interactions have not been studied; ask your doctor or pharmacist first.
Prescription drugs in general: the better-absorbed boswellic acids have not been checked for drug interactions in people; a pharmacist should review long-term use.
Pregnancy and breastfeeding: no safety data; avoid unless a doctor advises otherwise.

Frequently asked questions about Casperome® (Boswellia Phytosome — Indena)

What is Casperome?

Casperome® is Indena's Boswellia serrata gum resin extract bound to lecithin in a Phytosome® form, standardized to at least 25% triterpenoid acids. Boswellic acids are poorly absorbed from ordinary boswellia extracts, and the lecithin form was built to fix that: in a small crossover study in 12 healthy volunteers, most…

What is Casperome used for?

Casperome is researched primarily for Joint Health and Anti-Inflammatory. In a randomized, open-label crossover study in 12 healthy volunteers given 2 x 250 mg, the lecithin form produced significantly higher and faster blood levels of most boswellic acids than the same dose of plain extract; KBA was the exceptio…

What is the recommended dosage of Casperome?

The clinically studied dose is 250 mg once daily for 7 days in the ankle sprain registry study; one tablet daily for 6 months in an IBS study; 250 mg twice daily for 5 days in the diarrhea trial; 2 x 250 mg as a single dose in the absorption study. Always follow the product label and check with a healthcare provider for personal advice.

Is Casperome safe, and does it have side effects?

For most healthy adults, Casperome is well tolerated at studied doses. Reported effects can include: No relevant side effects were reported in the Casperome studies, which lasted from 5 days to 6 months. In the IBS studies, minor side effects such as constipation were less common with Casperome than with antispasmodic drugs. It may also interact with some medications. Casperome is not right for everyone, so check with a healthcare provider first if you are pregnant or breastfeeding, have a medical condition, or take prescription medication.

Does Casperome interact with any medications?

Possible interactions include: Pain relievers (NSAIDs): Casperome has not been formally tested with NSAIDs; ask your doctor before combining them. Blood thinners and antiplatelet drugs: interactions have not been studied; ask your doctor or pharmacist first. If you take prescription medication, check with a pharmacist or doctor before using it.

How strong is the scientific evidence for Casperome?

NutraSmarts rates the evidence for Casperome as Limited (2 out of 5). It is backed by 5 clinical trials and 8 cited references summarized on this page. A higher rating reflects more, larger, and better-designed human studies.

References(8 citations)

Evidence ratings on NutraSmarts are based on the totality of human clinical research, with emphasis on randomized controlled trials, meta-analyses, and systematic reviews. The references below directly support claims made throughout this page.

  1. Riva A, Morazzoni P, Artaria C, Allegrini P, Meins J, Savio D, Appendino G, Schubert-Zsilavecz M, Abdel-Tawab M A single-dose, randomized, cross-over, two-way, open-label study for comparing the absorption of boswellic acids and its lecithin formulation. Phytomedicine. 2016;23(12):1375-1382. doi: 10.1016/j.phymed.2016.07.009.PubMedUsed to support: In 12 healthy volunteers given 2 x 250 mg, Casperome gave significantly higher and faster absorption of boswellic acids than plain extract, except for KBA. Open-label; several authors work for Indena.
  2. Hüsch J, Bohnet J, Fricker G, Skarke C, Artaria C, Appendino G, Schubert-Zsilavecz M, Abdel-Tawab M Enhanced absorption of boswellic acids by a lecithin delivery form (Phytosome(®)) of Boswellia extract. Fitoterapia. 2013;84:89-98. doi: 10.1016/j.fitote.2012.10.002.PubMedUsed to support: Mouse study: Casperome, a soy lecithin form of boswellia extract, gave up to 7-fold higher plasma KBA and 3-fold higher β-boswellic acid than plain extract, with higher tissue levels. Animal data.
  3. Franceschi F, Togni S, Belcaro G, Dugall M, Luzzi R, Ledda A, Pellegrini L, Eggenhoffner R, Giacomelli L A novel lecithin based delivery form of Boswellic acids (Casperome®) for the management of osteo-muscular pain: a registry study in young rugby players. Eur Rev Med Pharmacol Sci. 2016;20(19):4156-4161..PubMedUsed to support: In 52 young rugby players with acute knee pain who chose their own group, Casperome plus standard care improved pain, walking distance, swelling and inflammatory markers more than standard care alone over 4 weeks. Open-label registry study, no placebo.
  4. Feragalli B, Ippolito E, Dugall M, Cacchio M, Belcaro G, Cesarone MR, Abdel-Tawab M, Riva A, Togni S, Eggenhoffner R, Giacomelli L Effectiveness of a novel boswellic acids delivery form (Casperome®) in the management of grade II ankle sprains due to sport trauma - a registry study. Eur Rev Med Pharmacol Sci. 2017;21(20):4726-4732..PubMedUsed to support: In 72 adults with grade II ankle sprains who chose their own group, 250 mg Casperome daily with standard care improved signs and symptoms at days 3 and 7 and lowered rescue drug use. Open-label pilot registry study, no placebo.
  5. Giacosa A, Riva A, Petrangolini G, Allegrini P, Fazia T, Bernardinelli L, Peroni G, Rondanelli M Positive Effects of a Lecithin-Based Delivery Form of Boswellia serrata Extract in Acute Diarrhea of Adult Subjects. Nutrients. 2022;14(9):1858. doi: 10.3390/nu14091858.PubMedUsed to support: Double-blind, placebo-controlled trial in 49 adults with acute diarrhea: 250 mg twice daily for 5 days shortened time to recovery (3.08 vs 4.44 days) and reduced stools, abdominal pain and nausea. Three authors are Indena employees.
  6. Riva A, Giacomelli L, Togni S, Franceschi F, Eggenhoffner R, Zuccarini MC, Belcaro G Oral administration of a lecithin-based delivery form of boswellic acids (Casperome®) for the prevention of symptoms of irritable bowel syndrome: a randomized clinical study. Minerva Gastroenterol Dietol. 2019;65(1):30-35. doi: 10.23736/S1121-421X.18.02530-8.PubMedUsed to support: In 69 adults with mild IBS followed for 6 months, one Casperome tablet daily led to lower symptom scores and fewer rescue medications and medical visits than standard antispasmodic care. No placebo or blinding; Indena and Belcaro group authors.
  7. Belcaro G, Gizzi G, Pellegrini L, Corsi M, Dugall M, Cacchio M, Feragalli B, Togni S, Riva A, Eggenhoffner R, Giacomelli L Supplementation with a lecithin-based delivery form of Boswellia serrata extract (Casperome®) controls symptoms of mild irritable bowel syndrome. Eur Rev Med Pharmacol Sci. 2017;21(9):2249-2254..PubMedUsed to support: Observational 4-week study in 71 adults with IBS: symptoms improved in all groups (Casperome or two antispasmodic drug regimens), with fewer medical visits and fewer side effects in the Casperome group. Preliminary, no placebo.
  8. Abdel-Tawab M, Werz O, Schubert-Zsilavecz M Boswellia serrata: an overall assessment of in vitro, preclinical, pharmacokinetic and clinical data. Clin Pharmacokinet. 2011;50(6):349-69. doi: 10.2165/11586800-000000000-00000.PubMedUsed to support: Review: AKBA and KBA reach very low blood levels after oral boswellia, so 5-lipoxygenase inhibition is a questionable main mechanism; β-boswellic acid, at much higher levels, inhibits microsomal prostaglandin E synthase-1 and cathepsin G.