Developer docs
API playgroundTry for free, no card

Search company profiles

PharmaMar (Zeltia Group)

Full company profile

uuid000d7ws

Namestring
PharmaMar (Zeltia Group)
Legal namestring
PharmaMar S.A.
Websiteurl
pharmamar.com
Company typeenum
Public
Founded yearint
1986
Descriptiontext

PharmaMar S.A., founded in 1986 and headquartered in Colmenar Viejo/Madrid, Spain, is a biopharmaceutical company that discovers, develops, and commercializes oncology therapeutics derived from marine organisms. The company operates the world's largest marine invertebrate compound library, comprising more than 550,000 samples gathered from over 200 marine expeditions, and has built an end-to-end development platform spanning compound isolation, chemical synthesis, preclinical studies, clinical trials, formulation, and manufacturing. Its core technology centers on marine-derived molecules with novel mechanisms of action — primarily selective inhibition of oncogenic transcription — and is augmented by a multi-agent AI system built with Globant that accelerates candidate identification from its compound library.

PharmaMar has three commercially approved drugs: Yondelis (trabectedin) for advanced soft tissue sarcoma and ovarian cancer; Zepzelca (lurbinectedin) for small cell lung cancer (SCLC), including the first-line maintenance combination with atezolizumab that received FDA full approval in October 2025 and EU approval in June 2026; and Aplidin (plitidepsin) for relapsed/refractory multiple myeloma in Australia. The pipeline includes ecubectedin (PM14), PM54, and PM534, each in Phase I for solid tumors, plus two RNAi-based ophthalmology assets (SYL1801 for nAMD; tivanisiran for Sjögren's dry eye) developed through subsidiary Sylentis. Manufacturing is concentrated at a 17,000 m² GMP-certified facility in Madrid approved by EMA, FDA, PMDA, and MFDS.

The company operates a hybrid commercial model: direct sales via wholly-owned subsidiaries in Germany, France, Italy, Belgium, Austria, Switzerland, and the United States, paired with regional licensing partnerships across more than 70 countries — including Jazz Pharmaceuticals (US/Canada), Merck (Japan), Immedica (Europe/MENA), Adium (Latin America), Luye Pharma (China), Specialised Therapeutics (Australia/SE Asia), Boryung (Korea), and Janssen (Yondelis US). Revenue is generated through direct product sales, royalties on partner sales, and milestone and licensing payments tied to regulatory and commercial events. The company is publicly listed on the Madrid Stock Exchange (BME:PHM) and operates as a subsidiary of Zeltia Group following a 2015 reverse merger.

Short descriptiontext

PharmaMar is a Madrid-based biopharmaceutical company that discovers, develops, and commercializes marine-derived oncology drugs, with three approved products (Yondelis, Zepzelca, Aplidin) sold globally via direct subsidiaries and licensing partners.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
251–500
akta.pro rankint
HeadquartersColmenar Viejo, Spain
HQ citystring
Colmenar Viejo
HQ countrystring
Spain
HQ regionstring
Europe
Markets served

Serves global market

Offices12 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
marine-derived oncology, anticancer drug development, marine biotechnology, orphan cancer therapies, biopharmaceutical research
Industry3 codes
1Oncology Specialty Pharmaceuticals
CodeHLAIACAAPrimaryYes
2Specialty Care Pharmaceuticals
CodeHLAIAAABPrimaryNo
3Ophthalmology Specialty Pharmaceuticals
CodeHLAIACAKPrimaryNo
NAICS code1 code
  • Pharmaceutical Preparation Manufacturing325412
SIC code1 code
  • Pharmaceutical Preparations2834
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model4 records
1Product Sales (Direct)
TypeHardware Sales
Description

Direct sales of approved oncology drugs (Yondelis, Zepzelca, Aplidin) through wholly-owned subsidiaries in Europe and US, with net sales generating revenue directly

in.investing.com
2Royalties from Partners
TypeLicensing Royalties
Description

Ongoing royalties received from partners including Jazz Pharmaceuticals, Janssen, and regional distributors based on their sales of licensed products

in.investing.com
3Milestone Payments
TypeLicensing Royalties
Description

One-time payments triggered by regulatory approvals and commercial milestones - received $50M from Jazz for FDA approval (Oct 2025), $25M first milestone, $10M from Janssen for Yondelis milestones

investing.com
4Licensing Fees
TypeLicensing Royalties
Description

Upfront and deal-based payments from licensing agreements - received $200M upfront from Jazz for lurbinectedina US rights, $100M upon FDA approval

investing.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels2 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components6 values
Technology or R&D, Personnel, Operations, Supply Chain, Infrastructure, Marketing or Sales
Pricing details1 tier
1Prescription oncology medications - pricing determined by regulatory and reimbursement frameworks
ModelOtherBilling cadenceMulti-year contract
Notes

Pricing varies by country based on healthcare system negotiations and reimbursement decisions. EU pricing approved by European Commission. US pricing subject to FDA and insurance frameworks.

pharmamar.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 3 records shown
1Yondelis
Description

Trabectedina - treatment for patients with advanced soft tissue sarcoma and ovarian cancer

pharmamar.com
+2 more records
Core offering1 text field

PharmaMar discovers, develops, manufactures, and commercializes oncology therapeutics derived from marine organisms. Its commercial portfolio includes Yondelis (trabectedin) for soft tissue sarcoma and ovarian cancer, Zepzelca (lurbinectedin) for small cell lung cancer (monotherapy and in combination with atezolizumab), and Aplidin (plitidepsin) for multiple myeloma. The company also operates subsidiary Sylentis, which develops RNAi-based ophthalmic therapies.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 5 values shown
  • 46% reduction in disease progression or death risk with Zepzelca + atezolizumab vs atezolizumab alone in first-line ES-SCLC (IMforte trial)
+4 more records
Product overview1 text field

PharmaMar is a global biopharmaceutical company pioneering marine-derived oncology therapeutics. The company operates with three commercially approved drugs: Yondelis (trabectedina) for soft tissue sarcoma and ovarian cancer, Zepzelca (lurbinectedina) for small cell lung cancer (as monotherapy and in combination with atezolizumab), and Aplidin (plitidepsina) for multiple myeloma in Australia. The pipeline includes Ecubectedina (PM14), PM54, and PM534 in clinical development for various solid tumors. Through subsidiary Sylentis, the company develops RNAi-based ophthalmic treatments including SYL1801 for macular degeneration and tivanisirán for dry eye disease. PharmaMar's approach spans the entire drug development lifecycle from marine expeditions and compound isolation to clinical trials and commercialization, supported by a multi-agent AI system for accelerated drug discovery.

Scale indicator15 records

Each record includes

Type, Value, Description, Source

Partnership19 partners
Strategic tierCoreTypeGTM or Marketing PartnerAnnounced on2026-06-23
Description

Licensing agreement for Yondelis (trabectedin) in US market. Received multiple milestone payments including $10M in November 2025 and previously in 2024, 2023, and 2022 for commercial milestones.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2026-03-19
Description

AI collaboration to develop multi-agent system for accelerating cancer drug discovery. System achieves 90%+ accuracy in data retrieval, 15x faster insights, processing 4,500+ research documents to identify 10 most viable candidates from 8,000+ possibilities. Next phase includes hypothesis generation and automated scientific reporting.

Strategic tierCoreTypeGTM or Marketing PartnerAnnounced on2025-04-03
Description

Exclusive licensing agreement for development and commercialization of Zepzelca (lurbinectedin) in Japan. PharmaMar announced submission of Japanese registration dossier with MHLW in June 2026.

Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2022-12-22
Description

TERINMUN research consortium for developing immunotherapies based on marine-derived compounds, in collaboration with Universidad Autónoma de Madrid.

Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2022-12-02
Description

ONCOLIBERYX consortium for developing novel drug delivery strategies for marine-derived oncology compounds with four Spanish research groups.

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2021-09-14
Description

Licensing agreement for Zepzelca commercialization in Australia, New Zealand, and Southeast Asia. Obtained approvals in Australia (2021, 2026 via Project Orbis) and Singapore (2026).

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2021-03-01
Description

Licensing agreement for Zepzelca commercialization across Latin America including Argentina, Bolivia, Brazil, Chile, Colombia, Costa Rica, Ecuador, El Salvador, Guatemala, Honduras, Jamaica, Mexico, Nicaragua, Panama, Paraguay, Peru, Dominican Republic, Trinidad and Tobago, Uruguay, Venezuela. Adium obtained approvals in Argentina, Peru, Mexico.

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2020-11-11
Description

Licensing agreement for Zepzelca commercialization in Taiwan. Obtained approval in Taiwan (March 2023, March 2026 for first-line).

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2020-05-11
Description

Licensing agreement for Zepzelca commercialization in Israel. Obtained approval in Israel (Jan 2023).

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2020-04-29
Description

Exclusive commercialization rights for Zepzelca in Eastern Europe, UK, Ireland, Nordic countries, and selected Middle East countries. Immedica obtained approvals in UAE, Switzerland, and coordinated EU approval via Project Orbis.

Strategic tierCoreTypeGTM or Marketing PartnerAnnounced on2019-12-19
Description

Exclusive licensing agreement for Zepzelca (lurbinectedin) commercialization in US and Canada. PharmaMar received $200M upfront, $100M upon FDA approval, $50M for full approval milestone (Oct 2025), and $25M first milestone payment. Jazz maintains 2026 guidance despite LAGOON trial failure. Deal included up to $1.008B in potential payments.

Strategic tierMinorTypeChannel Partner/ Reseller/ DistributorAnnounced on2019-09-12
Description

Licensing agreement for Zepzelca commercialization in South Africa, Namibia, Zimbabwe, Mozambique, Eswatini, Lesotho, and Botswana.

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2019-08-26
Description

Yondelis licensing agreements across Europe through various partners including R-Pharm (Russia/CIS), STADA (MENA), Eczacibasi (Turkey), Valeo Pharma (Canada), TTY Biopharm (Taiwan/HK/Macao), Key Oncologics (South Africa), STA (Australia/NZ/SE Asia), Megapharm (Israel).

Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2019-04-25
Description

Licensing agreement for lurbinectedin development and commercialization in China. Luye received approval in China (Dec 2024), Hong Kong (Dec 2023), and Macao (Dec 2023).

15Indonesia Oceanographic Research Center
Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2018-09-07
Description

MoU for collaboration in ocean research supporting marine biodiversity exploration for drug discovery.

pharmamar.com
Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2018-02-14
Description

Licensing of synthetic marine-derived molecules for use as antibody drug conjugates (ADCs) in cancer treatment.

17Huasin Science
Strategic tierMinorTypeChannel Partner/ Reseller/ DistributorAnnounced on2017-11-27
Description

Partnership for CLART diagnostic equipment production and distribution in Chinese market via GENOMICA.

pharmamar.com
Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2017-11-07
Description

Licensing agreement for Zepzelca commercialization in South Korea. Received approval in South Korea (Sept 2022).

Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2017-03-21
Description

Collaboration agreement to identify new marine-derived antitumor therapies through combined research efforts.

Recent move5 records

Each record includes

Date, Type, Title, Description, Source

Peers10 records
TypeBroad incumbent
Description

US specialty pharma that licenses and commercializes Zepzelca in US/Canada; overlapping oncology commercial infrastructure and SCLC focus. Both companies derive significant value from lurbinectedin, making Jazz the most economically linked peer.

TypeDirect peer
Description

Clinical-stage oncology specialty company with a partnered pipeline model (similar to PharmaMar's Jazz/Janssen structure) and ongoing Phase III catalysts. Comparable as a similarly scaled specialty oncology innovator reliant on partner-driven milestones.

TypeBroad incumbent
Description

Global oncology incumbent with a large SCLC franchise (Opdivo/Yervoy) and broad specialty pharma portfolio. Directly competes in the same indications PharmaMar targets and sets the standard of care that Zepzelca combinations are measured against.

TypeEmerging player
Description

China-rooted, globally active oncology specialty company with approved targeted therapies and a pipeline focused on hard-to-treat cancers. Comparable as a regionally anchored oncology innovator commercializing through partner networks, similar to PharmaMar's Luye partnership model.

TypeDirect peer
Description

Oncology specialty company with approved ADCs (Elahere) leveraging novel cytotoxic payloads derived from natural products — a directly comparable technological approach to PharmaMar's marine-derived chemistry in oncology.

TypeDirect peer
Description

Mid-cap US oncology specialty company with a focused commercial portfolio and pipeline, comparable in scale, business model (partner + direct sales), and reliance on a few key assets to drive revenue and royalties.

TypeDirect peer
Description

US oncology specialty company historically focused on SCLC (though smaller and financially constrained). Direct peer in lung cancer indication overlap, despite the differing commercial outcomes.

TypeBroad incumbent
Description

Specialty oncology company with a leading ADC platform that licensed PharmaMar's synthetic marine-derived molecules for ADC payloads. Comparable as an oncology specialty innovator leveraging natural-product inspired chemistry in a partnering-led commercial model.

TypeBroad incumbent
Description

Japan-headquartered global oncology company with marine-derived origins and a strong SCLC/ADC franchise (Enhertu). Operates as both a regional peer (Japan) and a comparable specialty oncology innovator with similar historical roots in natural-product discovery.

TypeBroad incumbent
Description

Owns atezolizumab (Tecentriq), the checkpoint inhibitor combined with Zepzelca in the IMforte regimen, and is the de facto commercial partner for Zepzelca's first-line indication. Comparable as a broad oncology incumbent and a co-dependency on PharmaMar's biggest commercial opportunity.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers1 record

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment2 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile1 record

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI capability4 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Subsidiaries10 records

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

Compliance3 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

PharmaMar (Zeltia Group)

PharmaMar is a Madrid-based biopharmaceutical company that discovers, develops, and commercializes marine-derived oncology drugs, with three approved products (Yondelis, Zepzelca, Aplidin) sold globally via direct subsidiaries and licensing partners.

What PharmaMar (Zeltia Group) does

PharmaMar S.A., founded in 1986 and headquartered in Colmenar Viejo/Madrid, Spain, is a biopharmaceutical company that discovers, develops, and commercializes oncology therapeutics derived from marine organisms. The company operates the world's largest marine invertebrate compound library, comprising more than 550,000 samples gathered from over 200 marine expeditions, and has built an end-to-end development platform spanning compound isolation, chemical synthesis, preclinical studies, clinical trials, formulation, and manufacturing. Its core technology centers on marine-derived molecules with novel mechanisms of action — primarily selective inhibition of oncogenic transcription — and is augmented by a multi-agent AI system built with Globant that accelerates candidate identification from its compound library.

PharmaMar has three commercially approved drugs: Yondelis (trabectedin) for advanced soft tissue sarcoma and ovarian cancer; Zepzelca (lurbinectedin) for small cell lung cancer (SCLC), including the first-line maintenance combination with atezolizumab that received FDA full approval in October 2025 and EU approval in June 2026; and Aplidin (plitidepsin) for relapsed/refractory multiple myeloma in Australia. The pipeline includes ecubectedin (PM14), PM54, and PM534, each in Phase I for solid tumors, plus two RNAi-based ophthalmology assets (SYL1801 for nAMD; tivanisiran for Sjögren's dry eye) developed through subsidiary Sylentis. Manufacturing is concentrated at a 17,000 m² GMP-certified facility in Madrid approved by EMA, FDA, PMDA, and MFDS.

The company operates a hybrid commercial model: direct sales via wholly-owned subsidiaries in Germany, France, Italy, Belgium, Austria, Switzerland, and the United States, paired with regional licensing partnerships across more than 70 countries — including Jazz Pharmaceuticals (US/Canada), Merck (Japan), Immedica (Europe/MENA), Adium (Latin America), Luye Pharma (China), Specialised Therapeutics (Australia/SE Asia), Boryung (Korea), and Janssen (Yondelis US). Revenue is generated through direct product sales, royalties on partner sales, and milestone and licensing payments tied to regulatory and commercial events. The company is publicly listed on the Madrid Stock Exchange (BME:PHM) and operates as a subsidiary of Zeltia Group following a 2015 reverse merger.

PharmaMar (Zeltia Group) firmographics

Firmographics
Name
PharmaMar (Zeltia Group)
Legal name
PharmaMar S.A.
Website
https://pharmamar.com
Company type
Public
Founded year
1986
Operating status
Operating
Headcount range
251–500 employees
Short description
PharmaMar is a Madrid-based biopharmaceutical company that discovers, develops, and commercializes marine-derived oncology drugs, with three approved products (Yondelis, Zepzelca, Aplidin) sold globally via direct subsidiaries and licensing partners.
Ownership category
akta.pro rank

PharmaMar (Zeltia Group) industry classification

Industry
NAICS
Pharmaceutical Preparation Manufacturing (325412)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Oncology Specialty Pharmaceuticals (HLAIACAA)
akta.pro secondary industries
Specialty Care Pharmaceuticals (HLAIAAAB), Ophthalmology Specialty Pharmaceuticals (HLAIACAK)

Keywords

  • Marine-derived oncology
  • Anticancer drug development
  • Marine biotechnology
  • Orphan cancer therapies
  • Biopharmaceutical research

Where PharmaMar (Zeltia Group) is headquartered

Location

Headquarters

HQ city
Colmenar Viejo
HQ country
Spain
HQ region
Europe

Offices12 records

Markets served

PharmaMar (Zeltia Group) business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Operations, Supply Chain, Infrastructure, Marketing or Sales

Revenue model

  1. Product Sales (Direct): Direct sales of approved oncology drugs (Yondelis, Zepzelca, Aplidin) through wholly-owned subsidiaries in Europe and US, with net sales generating revenue directly
  2. Royalties from Partners: Ongoing royalties received from partners including Jazz Pharmaceuticals, Janssen, and regional distributors based on their sales of licensed products
  3. Milestone Payments: One-time payments triggered by regulatory approvals and commercial milestones - received $50M from Jazz for FDA approval (Oct 2025), $25M first milestone, $10M from Janssen for Yondelis milestones
  4. Licensing Fees: Upfront and deal-based payments from licensing agreements - received $200M upfront from Jazz for lurbinectedina US rights, $100M upon FDA approval

Pricing tiers

ModelBillingPrice
OtherMulti-year contractPrescription oncology medications - pricing determined by regulatory and reimbursement frameworks

Go-to-market motion2 records

Distribution channels2 records

Marketing channels6 records

PharmaMar (Zeltia Group) product offering

Product offering

Core offering

PharmaMar discovers, develops, manufactures, and commercializes oncology therapeutics derived from marine organisms. Its commercial portfolio includes Yondelis (trabectedin) for soft tissue sarcoma and ovarian cancer, Zepzelca (lurbinectedin) for small cell lung cancer (monotherapy and in combination with atezolizumab), and Aplidin (plitidepsin) for multiple myeloma. The company also operates subsidiary Sylentis, which develops RNAi-based ophthalmic therapies.

Product overview

PharmaMar is a global biopharmaceutical company pioneering marine-derived oncology therapeutics. The company operates with three commercially approved drugs: Yondelis (trabectedina) for soft tissue sarcoma and ovarian cancer, Zepzelca (lurbinectedina) for small cell lung cancer (as monotherapy and in combination with atezolizumab), and Aplidin (plitidepsina) for multiple myeloma in Australia. The pipeline includes Ecubectedina (PM14), PM54, and PM534 in clinical development for various solid tumors. Through subsidiary Sylentis, the company develops RNAi-based ophthalmic treatments including SYL1801 for macular degeneration and tivanisirán for dry eye disease. PharmaMar's approach spans the entire drug development lifecycle from marine expeditions and compound isolation to clinical trials and commercialization, supported by a multi-agent AI system for accelerated drug discovery.

Differentiator

Problem solved

Functional benefit

Brands

  • Yondelis: Trabectedina - treatment for patients with advanced soft tissue sarcoma and ovarian cancer
  • Zepzelca
  • Aplidin

Quantifiable outcome

  • 46% reduction in disease progression or death risk with Zepzelca + atezolizumab vs atezolizumab alone in first-line ES-SCLC (IMforte trial)
  • +4 more outcomes

Companies that use PharmaMar (Zeltia Group)

Customer profile

Named customers1 record

Segments2 records

Ideal customer profiles1 record

PharmaMar (Zeltia Group) technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

AI capability4 records

Feature4 records

PharmaMar (Zeltia Group) partnerships and signals

Strategic signal

Partnerships

19 partnerships are on record, tiered core and minor.

  • Janssen Products LP (Johnson & Johnson)coreGTM or Marketing Partner · 23 June 2026Licensing agreement for Yondelis (trabectedin) in US market. Received multiple milestone payments including $10M in November 2025 and previously in 2024, 2023, and 2022 for commercial milestones.
  • GlobantcoreTechnology or Integration · 19 March 2026AI collaboration to develop multi-agent system for accelerating cancer drug discovery. System achieves 90%+ accuracy in data retrieval, 15x faster insights, processing 4,500+ research documents to identify 10 most viable candidates from 8,000+ possibilities. Next phase includes hypothesis generation and automated scientific reporting.
  • Merck (MRK.DE)coreGTM or Marketing Partner · 3 April 2025Exclusive licensing agreement for development and commercialization of Zepzelca (lurbinectedin) in Japan. PharmaMar announced submission of Japanese registration dossier with MHLW in June 2026.
  • Cima Universidad de NavarraminorStrategic or Co-development Partner · 22 December 2022TERINMUN research consortium for developing immunotherapies based on marine-derived compounds, in collaboration with Universidad Autónoma de Madrid.
  • Universidad Autónoma de MadridminorStrategic or Co-development Partner · 2 December 2022ONCOLIBERYX consortium for developing novel drug delivery strategies for marine-derived oncology compounds with four Spanish research groups.
  • Specialised Therapeutics Asia Pte. Ltd. (STA)coreChannel Partner/ Reseller/ Distributor · 14 September 2021Licensing agreement for Zepzelca commercialization in Australia, New Zealand, and Southeast Asia. Obtained approvals in Australia (2021, 2026 via Project Orbis) and Singapore (2026).
  • Adium Pharma S.A.coreChannel Partner/ Reseller/ Distributor · 1 March 2021Licensing agreement for Zepzelca commercialization across Latin America including Argentina, Bolivia, Brazil, Chile, Colombia, Costa Rica, Ecuador, El Salvador, Guatemala, Honduras, Jamaica, Mexico, Nicaragua, Panama, Paraguay, Peru, Dominican Republic, Trinidad and Tobago, Uruguay, Venezuela. Adium obtained approvals in Argentina, Peru, Mexico.
  • Lotus Pharmaceutical CO., Ltd.coreChannel Partner/ Reseller/ Distributor · 11 November 2020Licensing agreement for Zepzelca commercialization in Taiwan. Obtained approval in Taiwan (March 2023, March 2026 for first-line).
  • Megapharm Ltd.coreChannel Partner/ Reseller/ Distributor · 11 May 2020Licensing agreement for Zepzelca commercialization in Israel. Obtained approval in Israel (Jan 2023).
  • Immedica Pharma ABcoreChannel Partner/ Reseller/ Distributor · 29 April 2020Exclusive commercialization rights for Zepzelca in Eastern Europe, UK, Ireland, Nordic countries, and selected Middle East countries. Immedica obtained approvals in UAE, Switzerland, and coordinated EU approval via Project Orbis.
  • Jazz PharmaceuticalscoreGTM or Marketing Partner · 19 December 2019Exclusive licensing agreement for Zepzelca (lurbinectedin) commercialization in US and Canada. PharmaMar received $200M upfront, $100M upon FDA approval, $50M for full approval milestone (Oct 2025), and $25M first milestone payment. Jazz maintains 2026 guidance despite LAGOON trial failure. Deal included up to $1.008B in potential payments.
  • Key Oncologics (Pty) Ltd.minorChannel Partner/ Reseller/ Distributor · 12 September 2019Licensing agreement for Zepzelca commercialization in South Africa, Namibia, Zimbabwe, Mozambique, Eswatini, Lesotho, and Botswana.
  • Janssen (Yondelis Europe)coreChannel Partner/ Reseller/ Distributor · 26 August 2019Yondelis licensing agreements across Europe through various partners including R-Pharm (Russia/CIS), STADA (MENA), Eczacibasi (Turkey), Valeo Pharma (Canada), TTY Biopharm (Taiwan/HK/Macao), Key Oncologics (South Africa), STA (Australia/NZ/SE Asia), Megapharm (Israel).
  • Luye Pharma Group Ltd.coreChannel Partner/ Reseller/ Distributor · 25 April 2019Licensing agreement for lurbinectedin development and commercialization in China. Luye received approval in China (Dec 2024), Hong Kong (Dec 2023), and Macao (Dec 2023).
  • Indonesia Oceanographic Research CenterminorStrategic or Co-development Partner · 7 September 2018MoU for collaboration in ocean research supporting marine biodiversity exploration for drug discovery.
  • Seattle GeneticsminorStrategic or Co-development Partner · 14 February 2018Licensing of synthetic marine-derived molecules for use as antibody drug conjugates (ADCs) in cancer treatment.
  • Huasin ScienceminorChannel Partner/ Reseller/ Distributor · 27 November 2017Partnership for CLART diagnostic equipment production and distribution in Chinese market via GENOMICA.
  • Boryung CorporationcoreChannel Partner/ Reseller/ Distributor · 7 November 2017Licensing agreement for Zepzelca commercialization in South Korea. Received approval in South Korea (Sept 2022).
  • CNIO (Centro Nacional de Investigación Oncológica)minorStrategic or Co-development Partner · 21 March 2017Collaboration agreement to identify new marine-derived antitumor therapies through combined research efforts.

Scale indicators15 records

Recent moves5 records

PharmaMar (Zeltia Group) competitors and assessment

Company assessment

Broad incumbents

  • Jazz Pharmaceuticals: US specialty pharma that licenses and commercializes Zepzelca in US/Canada; overlapping oncology commercial infrastructure and SCLC focus. Both companies derive significant value from lurbinectedin, making Jazz the most economically linked peer.
  • Bristol-Myers Squibb: Global oncology incumbent with a large SCLC franchise (Opdivo/Yervoy) and broad specialty pharma portfolio. Directly competes in the same indications PharmaMar targets and sets the standard of care that Zepzelca combinations are measured against.
  • Seattle Genetics (Seagen / Pfizer): Specialty oncology company with a leading ADC platform that licensed PharmaMar's synthetic marine-derived molecules for ADC payloads. Comparable as an oncology specialty innovator leveraging natural-product inspired chemistry in a partnering-led commercial model.
  • Daiichi Sankyo: Japan-headquartered global oncology company with marine-derived origins and a strong SCLC/ADC franchise (Enhertu). Operates as both a regional peer (Japan) and a comparable specialty oncology innovator with similar historical roots in natural-product discovery.
  • AstraZeneca: Owns atezolizumab (Tecentriq), the checkpoint inhibitor combined with Zepzelca in the IMforte regimen, and is the de facto commercial partner for Zepzelca's first-line indication. Comparable as a broad oncology incumbent and a co-dependency on PharmaMar's biggest commercial opportunity.

Direct peers

  • MacroGenics: Clinical-stage oncology specialty company with a partnered pipeline model (similar to PharmaMar's Jazz/Janssen structure) and ongoing Phase III catalysts. Comparable as a similarly scaled specialty oncology innovator reliant on partner-driven milestones.
  • ImmunoGen: Oncology specialty company with approved ADCs (Elahere) leveraging novel cytotoxic payloads derived from natural products — a directly comparable technological approach to PharmaMar's marine-derived chemistry in oncology.
  • Exelixis: Mid-cap US oncology specialty company with a focused commercial portfolio and pipeline, comparable in scale, business model (partner + direct sales), and reliance on a few key assets to drive revenue and royalties.
  • Clovis Oncology: US oncology specialty company historically focused on SCLC (though smaller and financially constrained). Direct peer in lung cancer indication overlap, despite the differing commercial outcomes.

Emerging players

  • Hutchmed (China) Limited: China-rooted, globally active oncology specialty company with approved targeted therapies and a pipeline focused on hard-to-treat cancers. Comparable as a regionally anchored oncology innovator commercializing through partner networks, similar to PharmaMar's Luye partnership model.

Market position

Strengths5 records

Weaknesses5 records

Key risks6 records

Key highlights7 records

Customer concentration

PharmaMar (Zeltia Group) social profiles

Digital presence

PharmaMar (Zeltia Group) compliance and trust

Trust signal

Compliance3 records

PharmaMar (Zeltia Group) financial estimates

Financial estimate

Revenue estimate

Valuation estimate

PharmaMar (Zeltia Group) leadership team

Management profile

Number of profiles

PharmaMar (Zeltia Group) subsidiaries and ownership

Company hierarchy

Subsidiaries10 records

PharmaMar (Zeltia Group) funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

PharmaMar (Zeltia Group) M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about PharmaMar (Zeltia Group)

What does PharmaMar (Zeltia Group) do?

PharmaMar discovers, develops, manufactures, and commercializes oncology therapeutics derived from marine organisms. Its commercial portfolio includes Yondelis (trabectedin) for soft tissue sarcoma and ovarian cancer, Zepzelca (lurbinectedin) for small cell lung cancer (monotherapy and in combination with atezolizumab), and Aplidin (plitidepsin) for multiple myeloma. The company also operates subsidiary Sylentis, which develops RNAi-based ophthalmic therapies.

Is PharmaMar (Zeltia Group) a public or private company?

PharmaMar (Zeltia Group) is a public company. It is currently operating.

When was PharmaMar (Zeltia Group) founded?

PharmaMar (Zeltia Group) was founded in 1986. It employs 251 to 500 people.

Where is PharmaMar (Zeltia Group) based?

PharmaMar (Zeltia Group) is headquartered in Colmenar Viejo, Spain, in the Europe region.

How does PharmaMar (Zeltia Group) make money?

Four revenue lines are on record. Product Sales (Direct) is the primary driver. The others are royalties from Partners, milestone Payments and licensing Fees.

Who are PharmaMar (Zeltia Group)'s main competitors?

Broad incumbents on record are Jazz Pharmaceuticals, Bristol-Myers Squibb, Seattle Genetics (Seagen / Pfizer), Daiichi Sankyo and AstraZeneca. Direct peers are MacroGenics, ImmunoGen, Exelixis and Clovis Oncology. Hutchmed (China) Limited is listed as an emerging player.

Does PharmaMar (Zeltia Group) have an API?

No public API is recorded for PharmaMar (Zeltia Group).

What industry is PharmaMar (Zeltia Group) in?

Its primary akta.pro industry code is HLAIACAA, Oncology Specialty Pharmaceuticals, with a secondary code of HLAIAAAB, Specialty Care Pharmaceuticals. Its NAICS code is 325412 and its SIC code is 2834.

Unlock the full company data

50 free credits on sign-up, no credit card required.

Contact sales
Live signals
YahooPharma Mar (BME:PHM) Could Be 43% Undervalued After UK Zepzelca ApprovalThe UK MHRA approved Zepzelca plus atezolizumab as first-line maintenance therapy for extensive-stage small cell lung cancer, adding a new oncology market for Pharma Mar. The stock trades at €71.4, with a fair value of €125, implying a 43% undervaluation. Analysts expect European approval to boost revenues, though competition and regulatory risks remain.Simply Wall StIs Pharma Mar (BME:PHM) Cheap On Its New UK Zepzelca Approval?Pharma Mar's UK regulator approved Zepzelca with atezolizumab as first-line maintenance for extensive-stage small cell lung cancer. The stock trades at €73.1, with a fair value estimate of €125, implying undervaluation. Analysts expect European approval to boost revenues, though competition and pipeline reliance pose risks.PMLiVEMHRA approves Pharma Mar’s lurbinectedin for extensive-stage small cell lung cancerThe MHRA approved Pharma Mar's lurbinectedin for extensive-stage small cell lung cancer as maintenance after first-line therapy. In a study of 483 patients, the combination with atezolizumab gave median survival of 13.2 months versus 10.6 months for atezolizumab alone, and disease-free survival of 5.4 versus 2.1 months.Simply Wall StEuropean Growth Companies With Insider Ownership Up To 34%Simply Wall St profiles European growth companies with high insider ownership, including Pharma Mar, Kuros Biosciences, and Gold Road International. The list highlights insider stakes up to 35.9% and earnings growth forecasts, such as Kuros Biosciences at 58.6% and KebNi at 103.8%. The article also details NTG Nordic Transport Group and Morrow Bank, noting their insider ownership and growth projections.Ticker ReportPharma Mar (OTCMKTS:PHMMF) Short Interest UpdateShort interest in Pharma Mar surged 9,136.2% to 8,682 shares as of August 31st. Analysts rate the stock a consensus Buy, with Chardan Capital upgrading to strong-buy. The company develops marine-derived oncology therapies, including Yondelis.MarketScreenerPharma Mar Partner to File for Removal of Relapsed Small-cell Lung Cancer Indication from Zepzelca's Label in USPharma Mar, S.A. intends to file for the removal of the relapsed small-cell lung cancer indication from Zepzelca's label in the United States. This decision may reflect a strategic shift in the company's approach to their product offerings. The implications of this filing will be monitored closely as it could affect Zepzelca's market position and regulatory standing.PR NewswireSoft Tissue Sarcoma Market Set for Significant Growth at a CAGR of 7.9% During the Forecast Period (2026-2036), Driven by Novel Therapies and Expanding Treatment Landscape | DelveInsightThe soft tissue sarcoma market in the 7MM is projected to grow at a CAGR of 7.9% from 2026 to 2036, with the market size reaching USD 310 million in 2025. The United States accounted for approximately 85% of the total market size in 2025, and the incidence is expected to rise through 2036.PR NewswireSoft Tissue Sarcoma Market Set for Significant Growth at a CAGR of 7.9% During the Forecast Period (2026-2036), Driven by Novel Therapies and Expanding Treatment Landscape | DelveInsightThe soft tissue sarcoma market in the 7MM is projected to grow at a CAGR of 7.9% from 2026 to 2036, with the market size at USD 310 million in 2025. The United States accounted for approximately 85% of the total market size in 2025, and the incidence is expected to rise through 2036.Stock TitanJazz Pharma LAGOON trial misses survival goalJazz Pharmaceuticals announced that the Phase 3 LAGOON trial evaluating Zepzelca (lurbinectedin) for relapsed second-line small cell lung cancer did not meet its primary endpoint of overall survival, whether used as monotherapy or in combination with irinotecan compared to topotecan or irinotecan. The trial, sponsored by partner PharmaMar and enrolling 724 patients across more than 200 global sites, showed no new safety signals. The company noted that these results are distinct from the earlier IMforte trial that supported Zepzelca's 2025 first-line maintenance approval and will not impact 2026 guidance, though the FDA has been informed and next steps for the second-line indication will be discussed.news.cision.comZepzelca® (lurbinectedin) in combination with atezolizumab approved as first-line maintenance therapy for extensive-stage small cell lung cancer in United Arab Emirates (UAE)Immedica announced that the Emirates Drug Establishment has approved Zepzelca (lurbinectedin) in combination with atezolizumab as a first-line maintenance therapy for extensive-stage small cell lung cancer in the United Arab Emirates. This approval is based on Phase 3 IMforte trial results, which demonstrated significant reductions in disease progression and death risks compared to atezolizumab alone. Immedica holds the distribution rights for this product in the Middle East through a strategic partnership with PharmaMar.