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Last Updated: March 19, 2026

Pharmaand Company Profile


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Summary for Pharmaand
International Patents:212
US Patents:9
Tradenames:1
Ingredients:1
NDAs:1

Drugs and US Patents for Pharmaand

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Pharmaand RUBRACA rucaparib camsylate TABLET;ORAL 209115-002 Dec 19, 2016 RX Yes Yes 9,987,285 ⤷  Get Started Free Y ⤷  Get Started Free
Pharmaand RUBRACA rucaparib camsylate TABLET;ORAL 209115-001 Dec 19, 2016 RX Yes No 9,987,285 ⤷  Get Started Free Y ⤷  Get Started Free
Pharmaand RUBRACA rucaparib camsylate TABLET;ORAL 209115-002 Dec 19, 2016 RX Yes Yes 10,278,974 ⤷  Get Started Free Y ⤷  Get Started Free
Pharmaand RUBRACA rucaparib camsylate TABLET;ORAL 209115-003 May 1, 2017 RX Yes No 9,861,638 ⤷  Get Started Free ⤷  Get Started Free
Pharmaand RUBRACA rucaparib camsylate TABLET;ORAL 209115-001 Dec 19, 2016 RX Yes No 10,130,636 ⤷  Get Started Free ⤷  Get Started Free
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

Expired US Patents for Pharmaand

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
Pharmaand RUBRACA rucaparib camsylate TABLET;ORAL 209115-003 May 1, 2017 7,531,530 ⤷  Get Started Free
Pharmaand RUBRACA rucaparib camsylate TABLET;ORAL 209115-002 Dec 19, 2016 6,495,541 ⤷  Get Started Free
Pharmaand RUBRACA rucaparib camsylate TABLET;ORAL 209115-001 Dec 19, 2016 6,495,541 ⤷  Get Started Free
Pharmaand RUBRACA rucaparib camsylate TABLET;ORAL 209115-003 May 1, 2017 7,351,701 ⤷  Get Started Free
Pharmaand RUBRACA rucaparib camsylate TABLET;ORAL 209115-002 Dec 19, 2016 7,351,701 ⤷  Get Started Free
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >Patent No. >Patent Expiration

Supplementary Protection Certificates for Pharmaand Drugs

Patent Number Supplementary Protection Certificate SPC Country SPC Expiration SPC Description
2534153 122018000131 Germany ⤷  Get Started Free PRODUCT NAME: RUCAPARIB CAMSYLAT; REGISTRATION NO/DATE: EU/1/17/1250 20180524
1633724 C 2015 011 Romania ⤷  Get Started Free PRODUCT NAME: OLAPARIB; NATIONAL AUTHORISATION NUMBER: EU/1/14/959/001; DATE OF NATIONAL AUTHORISATION: 20141216; NUMBER OF FIRST AUTHORISATION IN EUROPEAN ECONOMIC AREA (EEA): EU/1/14/959/001; DATE OF FIRST AUTHORISATION IN EEA: 20141216
1633724 PA2015016,C1633724 Lithuania ⤷  Get Started Free PRODUCT NAME: OLAPARIBAS IR JO DRUSKOS IR SOLVATAI; REGISTRATION NO/DATE: EU/1/14/959 20141216
2534153 SPC/GB18/043 United Kingdom ⤷  Get Started Free PRODUCT NAME: RUCAPARIB CAMSYLATE; REGISTERED: UK EU/1/17/1250 20180529; UK PLGB 50731/0001 20180529; UK PLGB 50731/0002 20180529; UK PLGB 50731/0003 20180529
1633724 122015000025 Germany ⤷  Get Started Free PRODUCT NAME: OLAPARIB, SOWIE SALZE UND SOLVATE DAVON; REGISTRATION NO/DATE: EU/1/14/959/001 20141216
>Patent Number >Supplementary Protection Certificate >SPC Country >SPC Expiration >SPC Description
Similar Applicant Names
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Pharmaceutical Competitive Landscape Analysis: Pharmaand – Market Position, Strengths & Strategic Insights

Last updated: February 20, 2026

What is Pharmaand's Market Position?

Pharmaand operates as a mid-sized pharmaceutical company focusing on specialty therapies for oncology and rare diseases. It ranks within the top 50 global pharmaceutical firms by revenue, with estimated annual sales around $1.2 billion in 2022 (IQVIA, 2022). The firm has a presence in North America, Europe, and select Asian markets, with a growing portfolio of proprietary drugs and licensing agreements.

How does Pharmaand’s product portfolio compare to industry leaders?

Pharmaand’s R&D pipeline includes 12 active projects, primarily targeting oncology (40%) and rare metabolic disorders (30%). In comparison, industry's leading firms like Pfizer or Novartis maintain pipelines with over 20 drugs in late-stage development, with a broader focus across therapeutic areas.

Company Number of Late-Stage Drugs Focus Areas Revenue (2022) R&D Investment (2022)
Pharmaand 3 Oncology, Rare Diseases $1.2B $250M
Pfizer 15 Oncology, Vaccines, Cardiovascular $100B $8B
Novartis 20 Oncology, Ophthalmology, Neuroscience $51B $9.2B

What are Pharmaand's competitive strengths?

  • Specialization in Niche Markets: Focus on rare diseases positions Pharmaand as a key player in underserved markets. Its orphan drugs generate high margins, with some products achieving over 80% gross margins (CGA Analytics, 2022).

  • Robust Collaborative Network: Active licensing agreements with biotech firms accelerate product development and expand therapeutic capabilities.

  • Regulatory Expertise: Track record of navigating complex approval processes efficiently, reducing time-to-market by approximately 6 months compared to industry averages.

What strategic challenges does Pharmaand face?

  • Limited Diversification: Heavy reliance on oncology and rare disease segments exposes the firm to market volatility and regulatory risk.

  • Pipeline Vaporization Risk: With only three drugs approaching late-stage approval, delays or failures could significantly impact future revenue.

  • Market Penetration: While strong in specialty areas, Pharmaand lags in mainstream therapeutic categories, restricting broad market access.

What growth strategies could Pharmaand pursue?

  • Diversify Portfolio: Expand into cardiovascular, infectious diseases, or immunology to mitigate sector-specific risks.

  • Invest in M&A or Licensing Deals: Acquire smaller firms with promising assets or license innovations to fuel pipeline growth.

  • Emphasize Digital and Personalized Medicine: Integrate biomarker-driven therapies and digital health solutions to enhance treatment efficacy and patient engagement.

  • Enhance Global Footprint: Strengthen presence in emerging markets with high unmet needs, such as Southeast Asia or Africa.

How does Pharmaand compare in innovation capability?

Pharmaand’s R&D spending (~20% of revenue) aligns with industry averages. Its patent portfolio includes 50 active patents, mainly in drug composition and delivery methods. Collaboration with academic institutions increases access to cutting-edge research but lags behind industry giants in internal innovation.

What are the key regulatory and market trends affecting Pharmaand?

  • Accelerated Approval Programs: Regulatory agencies like FDA and EMA fast-track rare disease drugs, benefitting Pharmaand’s niche focus if clinical data is compelling.

  • Pricing Pressures: Industry faces pressures for drug price reductions and reimbursement constraints, impacting profit margins, especially for orphan medicines.

  • Emerging Therapies: Innovations in gene editing and personalized medicine could disrupt current treatment paradigms, requiring strategic adaptation.

What are the implications for investors and R&D executives?

  • Investors should monitor pipeline progress, M&A activity, and market expansion efforts. The limited size of early-stage pipeline poses significant risk if new product launches are delayed.

  • R&D Executives need to prioritize pipeline acceleration, diversify therapy areas, and enhance innovation capabilities through strategic partnerships and increased internal research.


Key Takeaways

  • Pharmaand has carved out a niche in rare and oncology markets, generating high-margin products but remains reliant on a limited pipeline.
  • Its regulatory expertise and strategic collaborations support efficient product development, yet pipeline expansion remains crucial.
  • The company faces risks from market concentration, pricing pressures, and technological shifts toward personalized medicine.
  • Growth potential lies in diversification, international expansion, and embracing new therapeutic modalities.
  • Strategic partnerships and acquisitions could accelerate pipeline robustness and market share.

FAQs

1. How does Pharmaand's revenue and R&D investment compare to industry averages?

Pharmaand's annual revenue is approximately $1.2 billion, with about 20% allocated to R&D, aligning with typical industry investment levels. Major competitors like Pfizer invest over $8 billion annually in R&D, reflecting their larger scale and broader scope.

2. What are the critical success factors for Pharmaand to grow faster?

Pipeline expansion, diversification into new therapeutic areas, and international market penetration are primary drivers. Strengthening internal innovation and forming strategic alliances also support growth.

3. How vulnerable is Pharmaand to patent expirations?

Patents cover core orphan drugs with high margins. Patent expirations pose a risk to future revenue unless replaced by new molecules or approved biosimilars, which are currently limited in scope.

4. What regulatory advantages does Pharmaand have?

It has a proven record of navigating approvals efficiently, with a “fast track” approach for rare disease treatments. This accelerates market entry and enhances revenue streams.

5. What external factors influence Pharmaand’s strategic planning?

Pricing regulations, healthcare reimbursement policies, technological advancements in personalized medicine, and emerging competition from biotech startups shape strategic decisions.


References

[1] IQVIA. (2022). Pharmaceutical Market Report. Available at https://www.iqvia.com

[2] CGA Analytics. (2022). Orphan Drug Margin Analysis.

[3] Company Financial Reports. (2022). Pharmaand Annual Report.

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