Last Updated: May 14, 2026

CLINICAL TRIALS PROFILE FOR SKELID


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All Clinical Trials for SKELID

Trial ID Title Status Sponsor Phase Start Date Summary
NCT01617057 ↗ Therapeutic Efficacy of Tiludronic Acid on Inner Ear Involvement in Advanced Otosclerosis Terminated Assistance Publique - Hôpitaux de Paris Phase 3 2012-05-01 The aim of this study is to assess the efficacy of a biphosphonate (tiludronic acid, Skelid®, Sanofi-Aventis) in the treatment of inner ear involvement in advanced otosclerosis
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for SKELID

Condition Name

Condition Name for SKELID
Intervention Trials
Otosclerosis 1
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Condition MeSH

Condition MeSH for SKELID
Intervention Trials
Otosclerosis 1
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Clinical Trial Locations for SKELID

Trials by Country

Trials by Country for SKELID
Location Trials
France 1
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Clinical Trial Progress for SKELID

Clinical Trial Phase

Clinical Trial Phase for SKELID
Clinical Trial Phase Trials
Phase 3 1
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Clinical Trial Status

Clinical Trial Status for SKELID
Clinical Trial Phase Trials
Terminated 1
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Clinical Trial Sponsors for SKELID

Sponsor Name

Sponsor Name for SKELID
Sponsor Trials
Assistance Publique - Hôpitaux de Paris 1
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Sponsor Type

Sponsor Type for SKELID
Sponsor Trials
Other 1
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Last updated: May 9, 2026

SKELID (clodronate) clinical trials update and market outlook

What is SKELID and how is it positioned commercially?

SKELID is the brand name for clodronic acid (oral formulation), used in bone resorption disorders such as bone metastases and other osteolytic conditions. The commercial profile of SKELID is defined by (1) an older, well-characterized bisphosphonate class, (2) multiple clodronate formulations available globally, and (3) a market driven by oncology supportive care and osteoporosis-adjacent use cases rather than curative intent.

Business implication: SKELID competes in a mature market segment where uptake depends less on differentiation and more on pricing, payer positioning, formulary access, and manufacturing continuity.

What is the latest clinical-trial signal for SKELID (clodronate)?

A current, drug-specific “clinical trials update” for SKELID requires a verifiable, SKELID-labeled clinical trial record (e.g., NCT entries explicitly tied to SKELID or clodronate at the SKELID dosage/form). Based on the information available in this session, no SKELID-specific trial dataset (identifiers, phases, endpoints, enrollment, or timelines) can be produced with the level of factual precision required.

Result: A complete and accurate SKELID clinical-trials update cannot be generated from the provided context.

How does SKELID’s clodronate class map to clinical use and trial patterns?

Clodronate (a first-generation bisphosphonate) typically appears in trial literature as:

  • A supportive-care intervention for bone metastases (often combined with cancer standard of care).
  • A bone resorption control agent in settings such as osteolysis.
  • A comparator against newer bisphosphonates or other antiresorptives in older trial generations.

Market effect: Trial activity for clodronate tends to be sparse in recent years relative to newer agents (e.g., denosumab and newer bisphosphonates) because clodronate’s efficacy is well established and the class faces shifting standards of care.


What is the current market landscape for clodronate brands like SKELID?

SKELID sits inside the bisphosphonate supportive-care market. Market dynamics for clodronate brands are shaped by:

  • Generic substitution pressure (clodronate is historically off-patent in most jurisdictions).
  • Physician familiarity and established prescribing habits in oncology supportive care.
  • Formulary access and reimbursement rules for bisphosphonates and supportive-care indications.
  • Competitive switching to alternatives with stronger guideline positioning in many regions (notably denosumab in some oncology bone disease contexts).

Key demand drivers

  • Incidence and prevalence of cancers with bone involvement, driving chronic or episodic supportive therapy needs.
  • Osteolytic activity management demand in oncology care pathways.
  • Cost containment: clodronate brands compete strongly on price and supply reliability.

Key headwinds

  • Generic erosion: brand pricing is constrained by interchangeable clodronate generics.
  • Guideline drift: newer antiresorptives change selection patterns in some indications and geographies.
  • Lower R&D velocity: limited justification for new pivotal programs when endpoints and mechanisms are mature.

What market share and revenue assumptions are implied for projection?

A market projection requires:

  • Country-by-country SKELID adoption curves (or at least a defined target geography).
  • Pricing trajectory, payer constraints, and generic penetration rates.
  • Clear specification of indication and dosing (units sold do not translate to revenue without this).

Result: A complete, evidence-based revenue projection cannot be produced from the information in this session because no SKELID-specific inputs (sales, geography, pricing, dosing, or tender/formulary data) are provided.


What investment-grade analytics can be generated from SKELID’s underlying class reality?

Even without SKELID-specific trial and sales inputs, the class economics support a structured outlook.

1) Patent and exclusivity posture (class-level expectation)

Clodronate is a legacy molecule; in most markets the active substance is generic. That typically produces:

  • Low probability of sustained “brand monopoly” revenue.
  • Reliance on localized brand presence, distribution reach, and reimbursement rather than exclusivity.

2) Competitive set

SKELID’s closest competitors in practice are:

  • Other clodronate products (brand vs brand, brand vs generic)
  • Other oral bisphosphonates (depending on indication and payer rules)
  • Non-bisphosphonate antiresorptives (in oncology bone disease contexts, especially where denosumab is preferred)

3) Forecast shape

For mature, mostly generic molecules, forecasting usually follows:

  • Plateau to slow decline in branded revenue
  • Occasional discrete step-changes from tender cycles, formulary decisions, and supply events

What should a decision-maker track for SKELID next?

Because SKELID-specific trial data and SKELID sales inputs are not present here, the highest-value next monitoring items are operational and policy driven:

  • Formulary inclusion changes for clodronate in oncology supportive care and bone resorption pathways.
  • Tender pricing dynamics and public procurement awards.
  • Generic entry waves in key markets (entry date, molecule form, dosing strength).
  • Safety surveillance outcomes that can influence prescribing behavior (class effects are established, but local label updates can move market behavior).

Key Takeaways

  • SKELID is a brand of clodronate (bisphosphonate) positioned in bone resorption and oncology supportive-care contexts.
  • A SKELID-specific clinical trials update (trial IDs, phase status, enrollment, endpoints, readouts) cannot be compiled from the available information in this session.
  • A market projection cannot be produced without SKELID-level commercial inputs (geography, dosing, pricing, sales base, generic penetration).
  • The most actionable outlook for SKELID is class-level: expect generic-driven pricing pressure, market dependence on formulary and tender outcomes, and low R&D throughput versus newer antiresorptives.

FAQs

1) Is SKELID likely to face strong generic competition?

Yes. Clodronate is a legacy bisphosphonate in markets where generic versions typically exist, which constrains branded pricing and volume.

2) What clinical settings typically use clodronate?

Bone resorption disorders and supportive oncology settings such as bone metastases/osteolytic activity management, depending on local labeling and guideline position.

3) Why is SKELID-focused new trial activity often limited?

The molecule is well characterized, and therapeutic standards for bone disease have shifted toward newer antiresorptives in many geographies, reducing incentives for new pivotal programs.

4) What drives SKELID demand in mature markets?

Formulary access, payer rules, oncology patient load with bone involvement, and procurement pricing.

5) What is the most realistic basis for forecasting SKELID revenue?

Tender and reimbursement-driven volume plus net pricing after generic competition, tracked by key geography and strength/formulation.


References

[1] No citable sources were provided in the prompt content.

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