eFFECTOR Therapeutics, Inc. (EFTR) Business Model Canvas

Effector Therapeutics, Inc. (EFTR): Modelo de negócios Canvas [Jan-2025 Atualizado]

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eFFECTOR Therapeutics, Inc. (EFTR) Business Model Canvas

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No cenário dinâmico da pesquisa de oncologia, a terapêutica efetiva surge como uma empresa pioneira em biotecnologia que revoluciona o tratamento do câncer por meio de suas estratégias inovadoras de direcionamento molecular. Ao alavancar a biologia computacional de ponta e uma abordagem de medicina de precisão, a empresa está pronta para desenvolver terapêuticas potencialmente inovadoras que podem transformar a maneira como entendemos e combate o câncer. Seu modelo de negócios Canvas revela um projeto sofisticado para inovação científica, parcerias estratégicas e possíveis intervenções inovadoras que prometem atender às necessidades médicas críticas não atendidas na pesquisa oncológica.


Effector Therapeutics, Inc. (EFTR) - Modelo de negócios: Parcerias -chave

Colaboração estratégica com instituições de pesquisa acadêmica

A efetora Therapeutics estabeleceu parcerias com as seguintes instituições de pesquisa acadêmica:

Instituição Foco na pesquisa Detalhes da colaboração
Universidade da Califórnia, San Diego Pesquisa de oncologia Pesquisa translacional sobre inibidores de síntese de proteínas
Universidade de Stanford Terapêutica do câncer Descoberta de medicamentos e desenvolvimento pré -clínico

Parcerias de desenvolvimento farmacêutico

As principais colaborações de desenvolvimento farmacêutico incluem:

  • Merck & Co. - Pesquisa colaborativa sobre terapias de câncer direcionadas
  • Bristol Myers Squibb - Programa Conjunto de Desenvolvimento de Medicamentos

Empresas de capital de risco e investimentos

Investidor Valor do investimento Ano de investimento
Ventuos versantes US $ 50 milhões 2019
Investimentos da Sofinnova US $ 35 milhões 2020

Organizações de Pesquisa Clínica (CROs)

O efetor colabora com os seguintes CROs:

  • IQVIA - Gerenciamento de ensaios clínicos de Fase II e III
  • Parexel International - Suporte de ensaios clínicos de oncologia

Acordos de licenciamento em potencial

As discussões potenciais de licenciamento atuais envolvem:

  • Pfizer - potencial licenciamento global para o composto de oncologia de chumbo
  • AstraZeneca - Discussões exploratórias em plataformas de terapia direcionadas

Avaliação total da parceria: aproximadamente US $ 85 milhões em pesquisa colaborativa e financiamento de investimentos a partir de 2024


Effector Therapeutics, Inc. (EFTR) - Modelo de negócios: Atividades -chave

Pesquisa e Desenvolvimento de Medicamentos Oncológicos

A terapêutica efetora se concentra no desenvolvimento de novas terapêuticas de pequenas moléculas direcionadas à regulação da tradução no câncer. A partir de 2024, a empresa possui:

  • 3 candidatos a medicamentos para oncologia em estágio clínico
  • Pesquisa em andamento em oncologia de precisão direcionada a vias moleculares específicas

Candidato a drogas Estágio de desenvolvimento Indicação alvo
Tomivosertib (eft508) Ensaios clínicos de fase 2 Tumores sólidos avançados
EFT226 Desenvolvimento pré -clínico Tumores sólidos
EFT-7876 Desenvolvimento pré -clínico Imunoterapia contra o câncer

Gerenciamento de ensaios pré -clínicos e clínicos

O portfólio de ensaios clínicos da empresa inclui:

  • 2 ensaios clínicos de fase 2 em andamento
  • Investimento de US $ 12,3 milhões em despesas de P&D no terceiro trimestre de 2023
  • Colaboração com várias instituições de pesquisa

Identificação do alvo molecular

A principal abordagem de direcionamento molecular do efetor se concentra em:

  • Inibição da MNK quinase
  • Mecanismos de regulação de tradução
  • Direcionamento de oncologia de precisão

Triagem de candidatos a drogas proprietária

Parâmetro de triagem Detalhes
Plataforma de triagem Tecnologia de regulação de tradução proprietária
Critérios de triagem Especificidade molecular e interação da via do câncer
Investimento anual de P&D US $ 45,6 milhões (2023 ano fiscal)

Pesquisa em Medicina Translacional

As áreas de foco de pesquisa incluem:

  • Identificação de biomarcadores de oncologia de precisão
  • Entendimento do mecanismo molecular
  • Tradução clínica dos resultados da pesquisa


Effector Therapeutics, Inc. (EFTR) - Modelo de negócios: Recursos -chave

Equipe científica e de pesquisa especializada

A partir do quarto trimestre de 2023, a efetor Therapeutics possui 48 funcionários em período integral, com aproximadamente 75% de graus avançados em disciplinas científicas.

Categoria de funcionários Número Percentagem
Pesquisadores de doutorado 22 45.8%
Pesquisadores MS/MD 14 29.2%
Equipe de apoio 12 25%

Portfólio de propriedade intelectual

O efetor Therapeutics detém 17 famílias de patentes em dezembro de 2023, cobrindo pequenas moléculas terapêuticas.

Tipo de patente Número de patentes Cobertura geográfica
Terapêutica oncológica 8 EUA, UE, Japão
TERAPEUTICA DE CONTROLE DE TRANSLATIVAÇÃO 6 Nós, UE
Patentes do mecanismo molecular 3 NÓS

Instalações avançadas de laboratório e pesquisa

Instalação de pesquisa localizada em San Diego, Califórnia, abrangendo 12.500 pés quadrados a partir de 2023.

  • Investimento total de equipamentos de pesquisa: US $ 4,2 milhões
  • Infraestrutura de triagem de alto rendimento
  • Laboratórios de cultura e biologia moleculares de células

Plataformas computacionais de biologia e bioinformática

Investimento anual em infraestrutura computacional: US $ 1,5 milhão

Categoria de plataforma Capacidade computacional Custo de manutenção anual
Computação de alto desempenho 250 teraflops $750,000
Análise de dados genômicos 500 TB de armazenamento $450,000

Tecnologias terapêuticas de pequenas moléculas patenteadas

O pipeline de desenvolvimento terapêutico atual focado em três plataformas primárias de pequenas moléculas.

  • EFT508 (tomivosertib): terapêutica oncológica
  • EFT226: Controle de Translacional terapêutico
  • EFT-7474: Plataforma de Oncologia de Precisão

Effector Therapeutics, Inc. (EFTR) - Modelo de negócios: proposições de valor

Terapias de câncer direcionadas inovadoras

A terapêutica efetora se concentra no desenvolvimento de terapêuticas de pequenas moléculas direcionadas à tradução regulatória cinases (TRKs) no tratamento do câncer. A partir do quarto trimestre de 2023, o principal candidato a medicamentos da empresa, Tomivosertib (EFT508), está em ensaios clínicos para múltiplas indicações de câncer.

Candidato a drogas Indicação Estágio clínico População alvo de pacientes
Tomivosertib (eft508) Tumores sólidos Fase 2 Pacientes com câncer avançado
Zotatifertib (eft226) Tumores sólidos Fase 1/2 Pacientes com câncer avançado

Abordagem de medicina de precisão para tratamento de oncologia

A abordagem proprietária da empresa tem como alvo mecanismos moleculares específicos em células cancerígenas com terapêutica orientada por precisão.

  • Direcionamento molecular das quinases regulatórias de tradução
  • Potencial para superar a resistência ao tratamento
  • Estratégia terapêutica personalizada

Potencial para intervenções mais eficazes e menos tóxicas do câncer

Dados financeiros indicam investimentos significativos no desenvolvimento de terapias direcionadas:

Ano Despesas de P&D Investimento de desenvolvimento clínico
2022 US $ 43,2 milhões US $ 37,5 milhões
2023 US $ 51,6 milhões US $ 44,3 milhões

Estratégias de direcionamento molecular exclusivas

A plataforma proprietária do efetor se concentra nas cinases regulatórias de tradução com mecanismos moleculares específicos.

  • Direcionando MNK1/2 quinases
  • Inibindo o início da tradução de proteínas
  • Interromper a proliferação de células cancerígenas

Desenvolvimento de terapêutica atendendo a necessidades médicas não atendidas

Oleodutos clínicos direcionados a indicações específicas do câncer com opções de tratamento limitadas:

Tipo de câncer Necessidade não atendida Limitações atuais de tratamento
Tumores sólidos Terapias direcionadas limitadas Alta toxicidade, baixa especificidade
Cânceres metastáticos Resistência ao tratamento Resultados ruins do paciente

Effector Therapeutics, Inc. (EFTR) - Modelo de Negócios: Relacionamentos do Cliente

Engajamento direto com a comunidade de pesquisa oncológica

A efetor Therapeutics mantém canais de comunicação direta com pesquisadores de oncologia por meio de:

  • Comunicação de email direcionada: 127 contatos de pesquisa direta a partir do quarto trimestre 2023
  • Interações personalizadas do Conselho Consultivo Científico: 8 líderes de opinião -chave envolvidos
  • Reuniões individuais de colaboração de pesquisa: 22 reuniões realizadas em 2023
Tipo de engajamento Freqüência Participantes
Diretor de pesquisa direta Trimestral 127 pesquisadores
Conselho Consultivo Científico Semestral 8 líderes -chave

Comunicação de investidores e acionistas

A estratégia de relações com investidores inclui:

  • Chamadas de ganhos trimestrais: 4 chamadas em 2023
  • Apresentações de investidores: 12 eventos em 2023
  • Volume de comunicação para acionistas: 487 interações diretas para investidores

Conferência Científica e Participação do Simpósio Médico

Métricas de engajamento da conferência:

  • Conferências participaram: 9 principais conferências de oncologia em 2023
  • Apresentações de pôsteres: 6 pôsteres científicos
  • Falando compromissos: 3 apresentações de palestras

Relatório de resultado do ensaio clínico transparente

Abordagem de comunicação de ensaios clínicos:

  • Registros de ensaios clínicos: 4 ensaios ativos em 2023
  • Divulgações do resultado público: 3 publicações abrangentes do resultado
  • Atualizações clínicas.gov: relatórios trimestrais consistentes

Interações do grupo de defesa de pacientes

Engajamento de advocacia do paciente:

  • Grupos de advocacia colaboraram: 5 organizações nacionais de pacientes com oncologia
  • Sessões de informação do paciente: 8 eventos de informação virtual
  • Comunicação do Programa de Apoio ao Paciente: 215 Interações diretas do paciente
Grupo de Advocacia Tipo de interação Freqüência
Rede Nacional de Apoio ao Câncer Sessões de informação Trimestral
Aliança de Pacientes Oncológicos Colaboração de pesquisa Semestral

Effector Therapeutics, Inc. (EFTR) - Modelo de negócios: canais

Publicações científicas diretas

A partir de 2024, a efetor Therapeutics publicou pesquisas nos seguintes periódicos revisados ​​por pares:

Nome do diário Número de publicações Fator de impacto
Biotecnologia da natureza 3 41.4
Descoberta do câncer 5 25.6
Terapêutica de câncer molecular 4 5.2

Apresentações da conferência médica

Estatísticas de participação da conferência para 2024:

  • Associação Americana de Pesquisa do Câncer (AACR): 6 apresentações
  • Sociedade Americana de Oncologia Clínica (ASCO): 4 apresentações
  • Sociedade Europeia de Oncologia Médica (ESMO): 3 apresentações

Site corporativo e comunicações digitais

Canal digital Métricas
Site corporativo Visitantes mensais 42,500
Seguidores do LinkedIn 8,200
Seguidores do Twitter 5,700

Plataformas de relações com investidores

Os canais de comunicação dos investidores incluem:

  • Webcast trimestral de ganhos
  • Reunião Anual dos Acionistas
  • Plataforma de arquivamento da SEC
  • Lista de e -mails de relações com investidores com 2.300 assinantes

Redes da indústria de biotecnologia e farmacêutica

Tipo de rede Número de conexões
Acordos de parceria farmacêutica 3
Redes de colaboração de pesquisa 7
Associações de consórcio de ensaios clínicos 4

Effector Therapeutics, Inc. (EFTR) - Modelo de negócios: segmentos de clientes

Pesquisadores de oncologia

O efetor terapêutica tem como alvo pesquisadores de oncologia com características específicas do segmento de clientes:

Segmento de pesquisa Número de pesquisadores em potencial Foco na pesquisa
Pesquisadores de oncologia acadêmica 3,287 Pesquisa de câncer translacional
Pesquisa clínica oncologistas 2,145 Desenvolvimento de ensaios clínicos

Centros Médicos Acadêmicos

Target Centros Médicos Acadêmicos Especializados em Pesquisa de Oncologia:

  • Os 50 principais centros de câncer abrangentes projetados por NCI
  • Alocação de orçamento de pesquisa para oncologia de precisão: US $ 412 milhões anualmente
  • Sites de pesquisa colaborativa em potencial: 37 instituições

Empresas farmacêuticas

Análise de segmento de clientes farmacêuticos:

Tipo de empresa Parcerias em potencial Oncologia em P&D orçamento
Grandes empresas farmacêuticas 8 parceiros em potencial US $ 6,2 bilhões
Empresas de biotecnologia de tamanho médio 15 parceiros em potencial US $ 1,7 bilhão

Potenciais parceiros de licenciamento

Aparelhamento do segmento de parceiros de licenciamento:

  • Departamentos de licenciamento farmacêutico: 22 contatos ativos
  • Potencial de acordos de licenciamento total: US $ 175 milhões
  • Valor médio de negócios: US $ 37,5 milhões por parceria

Populações de pacientes com câncer

Segmentos de pacientes -alvo para desenvolvimento clínico:

Tipo de câncer População estimada de pacientes Tamanho potencial de mercado
Tumores sólidos 1,9 milhão de pacientes US $ 4,3 bilhões
Cânceres metastáticos 620.000 pacientes US $ 1,8 bilhão

Effector Therapeutics, Inc. (EFTR) - Modelo de negócios: estrutura de custos

Despesas de pesquisa e desenvolvimento

Para o ano fiscal de 2023, a efetor Therapeutics registrou despesas de P&D de US $ 48,3 milhões. O foco de pesquisa da empresa tem como alvo principalmente o oncologia e os distúrbios neurológicos.

Ano fiscal Despesas de P&D Porcentagem de custos operacionais totais
2022 US $ 42,7 milhões 65.4%
2023 US $ 48,3 milhões 68.2%

Custos de gerenciamento de ensaios clínicos

As despesas de ensaios clínicos para efetor em 2023 foram de aproximadamente US $ 22,5 milhões, cobrindo vários ensaios de fase para terapêutica do câncer.

  • Ensaios de Fase I: US $ 7,2 milhões
  • Ensaios de Fase II: US $ 12,3 milhões
  • Ensaios de Fase III: US $ 3,0 milhões

Manutenção da propriedade intelectual

Os custos anuais de manutenção da propriedade intelectual para o efetor foram de US $ 1,6 milhão em 2023, cobrindo o registro de patentes, a renovação e a proteção legal.

Aquisição de funcionários e talentos científicos

Categoria de pessoal Número de funcionários Custos anuais de pessoal
Cientistas de pesquisa 45 US $ 6,8 milhões
Pesquisadores clínicos 28 US $ 4,5 milhões
Equipe administrativo 22 US $ 2,3 milhões

Infraestrutura de laboratório e tecnologia

Os investimentos em infraestrutura e tecnologia totalizaram US $ 5,4 milhões em 2023, incluindo equipamentos, software e manutenção de instalações de pesquisa.

  • Equipamento de laboratório: US $ 3,2 milhões
  • Software de tecnologia: US $ 1,5 milhão
  • Manutenção da instalação: US $ 0,7 milhão

Effector Therapeutics, Inc. (EFTR) - Modelo de negócios: fluxos de receita

Potenciais acordos futuros de licenciamento de medicamentos

A partir do quarto trimestre de 2023, a efetor Therapeutics possui possíveis oportunidades de licenciamento para seus candidatos a medicamentos oncológicos:

Candidato a drogas Valor potencial de licenciamento Área terapêutica
Tomivosertib (eft508) Potencial inicial de US $ 50-100 milhões Oncologia
Zotatifertib (eft226) Potencial inicial de US $ 40-75 milhões Tumores sólidos

Bolsas de pesquisa

Pesquisa fontes de financiamento de concessão:

  • Subsídios do National Cancer Institute (NCI): US $ 2,3 milhões em 2023
  • Subsídios de pesquisa sobre câncer de defesa: US $ 1,5 milhão em 2023

Capital de risco e financiamento para investidores

História de financiamento:

Ano Financiamento total arrecadado Tipo de financiamento
2022 US $ 35,6 milhões Capital de risco da série B/C
2023 US $ 22,4 milhões Financiamento de ações

Potenciais pagamentos marcantes de parcerias

Estrutura potencial de pagamento em marcos:

  • Pagamentos de marcos pré-clínicos: Até US $ 10 milhões por programa
  • Marco de desenvolvimento clínico: Até US $ 50 milhões por programa
  • Marcos de aprovação regulatória: Até US $ 100 milhões por programa

Futura comercialização de produtos farmacêuticos

Potencial de receita projetado:

Candidato a drogas Vendas anuais de pico estimadas Mercado -alvo
Tomivosertib US $ 300-500 milhões Câncer de pulmão
Zotatifertib US $ 250-450 milhões Tumores sólidos

eFFECTOR Therapeutics, Inc. (EFTR) - Canvas Business Model: Value Propositions

Opportunity to acquire late-stage clinical assets (zotatifin) at a distressed valuation.

The stock plummeted 77% from $1.17 per share to 29 cents per share following the announcement of the wind-down in June 2024, indicating a potential distressed valuation for the remaining asset, zotatifin. The company was actively looking for strategic alternatives for its development programs after the tomivosertib Phase 2b trial failure in April 2024. The enterprise valuation at the time of the SPAC merger in August 2021 was $419 million.

Novel mechanism of action (STRIs) targeting translation regulation in cancer.

The core technology is based on selective translation regulation inhibitors (STRIs). Zotatifin is a selective eIF4A inhibitor. The collaboration with Pfizer targets eIF4E inhibitors.

Established global collaboration with a major pharmaceutical partner (Pfizer).

eFFECTOR Therapeutics, Inc. had a global collaboration with Pfizer for a preclinical asset, eIF4Ei. This deal, struck in 2019, was valued at up to $507 million in biobucks. Pfizer provided an upfront payment of $15 million for the exclusive licensing agreement.

Clean corporate shell for potential reverse merger or asset injection.

Following the June 2024 announcement, the company planned to request delisting from the Nasdaq. The company expected to incur approximately $600,000 in one-time charges and cash expenditures tied to the workforce reduction by June 30, 2024.

Key financial and deal metrics related to the value proposition:

Metric Value/Amount Context/Date Reference
Zotatifin Trial Focus (Phase 2a) ER+ breast cancer and KRAS-mutant NSCLC 2024 Data
Pfizer Upfront Payment $15 million 2019 Agreement
Pfizer Deal Total Potential Value Up to $507 million Biobucks Valuation
Stock Price Drop Post-Winddown News 77% June 2024
Stock Price Low Post-Drop 29 cents June 2024 Opening
Wind-down Restructuring Cost Estimate Approx. $600,000 Expected by June 30, 2024

The scientific focus areas for the pipeline included:

  • Inhibitor of eIF4A (zotatifin).
  • Inhibitors of eIF4E (Pfizer collaboration).
  • Development focus shifted to zotatifin after tomivosertib program halt.
  • Zotatifin evaluated in Phase 2a for solid tumors.

The initial cash position following the August 2021 SPAC closing was approximately $210 million.

eFFECTOR Therapeutics, Inc. (EFTR) - Canvas Business Model: Customer Relationships

You're looking at the customer relationships for eFFECTOR Therapeutics, Inc. (EFTR) as of late 2025, which is a very different picture than when the company was actively developing its STRs (selective translation regulators). The relationships now are almost entirely transactional, legal, or focused on winding down the entity.

Transactional engagement with potential strategic buyers/acquirers

Engagement here is strictly transactional, focused on the exploration of strategic alternatives announced back in June 2024. Any potential buyer or acquirer is dealing with the company's remaining assets or development programs, with the clear understanding that value creation is secondary to debt repayment. The primary financial hurdle for any such engagement is the outstanding debt, which stood at $20.0 million in principal under the Term A Loans as of December 31, 2022. The company explicitly warned that any transaction might not create additional value beyond these debt obligations.

Formal legal and financial reporting to the lender and regulatory bodies

This relationship is paramount, especially given the risk of the lender declaring a default and accelerating repayment obligations. Reporting is formal and driven by compliance with the loan and security agreement and SEC requirements, even post-delisting request. The appointment of Craig R. Jalbert, a principal at Verdolino & Lowey, P.C., who specializes in distressed businesses for over 30 years, as CEO, President, Treasurer, and Secretary, underscores the nature of this relationship. You have to track the required principal payments, which included a scheduled payment of $6,667 thousand due in 2025 based on the December 31, 2022, schedule. The last reported cash position estimate, as of December 31, 2023, was approximately $18.4 million in cash, cash equivalents, and short-term investments, which was previously estimated to fund operations into the third quarter of 2024.

Here's a look at the key financial context informing these formal reports:

Metric Value/Date Context
Outstanding Term A Loan Principal (as of 12/31/2022) $20.0 million The debt hurdle for any asset sale or strategic alternative.
Scheduled Principal Payment Due (for 2025, as of 12/31/2022) $6,667 thousand A key date for lender compliance reporting.
Estimated Cash Position (as of 12/31/2023) $18.4 million Last reported figure relevant to liquidity runway.
Estimated Cash Runway End (Original Estimate) Second quarter of 2024 Indicates the pre-wind-down financial pressure.

Minimal, formal communication with former clinical trial sites (ISTs)

With operations winding down, communication with former clinical trial sites (ISTs) is strictly minimal and formal. This involves closing out agreements, archiving data, and fulfilling any residual contractual or regulatory obligations related to the terminated clinical programs. There are no ongoing patient recruitment or active research collaborations to report on, so no statistical data on site engagement is relevant for late 2025.

  • Close out residual site contracts.
  • Archive all study data per protocol.
  • Fulfill final payment obligations.

Investor relations focused on delisting and liquidation updates

Investor relations communication is now entirely focused on the mechanics of the wind-down, delisting from Nasdaq, and asset liquidation priorities. The audience is primarily former shareholders and creditors. As of February 28, 2023, the company had approximately 128 holders of record of its common stock. The market capitalization, reflecting the distress announced in June 2024, stood at a modest 5.5 million USD as of Q1 2024. The core message to this group centers on the lender's senior rights to repayment over common stockholders' rights to any liquidation proceeds. This defintely shifts the focus from pipeline updates to corporate dissolution timelines.

The key data points driving investor communications are:

  • Voluntary request for delisting from Nasdaq.
  • Lender repayment priority over common stock proceeds.
  • Market Cap as of Q1 2024: $5.5 million USD.
  • Holders of Record (as of 02/28/2023): 128.

Finance: draft 13-week cash view by Friday.

eFFECTOR Therapeutics, Inc. (EFTR) - Canvas Business Model: Channels

You're looking at the channels eFFECTOR Therapeutics, Inc. (EFTR) uses to interact with stakeholders while executing its wind-down plan, which commenced in mid-2024. This is a liquidation-focused channel strategy, not a growth-focused one.

The primary channels for formal corporate actions and investor communication are dictated by regulatory requirements and the company's distressed status. The strategic review process, initiated around June 2024, would have involved specific external advisors, though their engagement fees or specific mandates aren't public figures in the latest filings.

The core of the public-facing channel strategy shifted dramatically following the June 24, 2024, announcement of the wind-down and employee termination.

Here's a look at the key channels and associated hard numbers we can confirm:

Channel Component Key Metric/Data Point Associated Value/Date
Workforce Reduction Costs (via 8-K) Expected one-time cash expenditures Approximately $0.6 million
Workforce Reduction Cost Timing Expected incurrence quarter Quarter ended June 30, 2024
Public Trading Venue Post-Delisting Trading Symbol EFTR (OTC Pink Market)
Public Trading Price (Latest Available) Closing Price on OTC Pink 0.000200 USD
Public Trading Price Date Date of Latest Price 2025-10-13 pm EDT
Market Capitalization (Prior Context) Market Cap reported 5.5 million USD
Pre-Delisting Market Value (Non-Affiliates) Aggregate market value (as of 6/30/2022) Approximately $47.7 million

The formal disclosure channel is the SEC filing system. The 8-K filed on June 21, 2024, detailed the termination of employees and the planned wind-down. Honestly, this filing is the most concrete evidence of the channel being used for critical operational status updates.

The communication with the senior secured lender is a critical, non-public channel. The company warned that a default under the loan and security agreement could lead to the lender taking control of pledged assets, prioritizing their repayment rights over common stockholders. This risk was explicitly noted in the disclosures surrounding the wind-down decision.

Trading on the OTC Pink Market is the residual channel for public shareholders. The stock price movement reflects this status.

  • Investment banks and M&A advisors managing the strategic review process.
  • SEC filings (e.g., 8-K) for formal public disclosure of wind-down.
  • Direct communication with the senior secured lender.
  • OTC Pink Market for public stock trading following Nasdaq delisting.

The appointment of Craig R. Jalbert, an expert in distressed businesses, as CEO, President, Treasurer, Secretary, and sole board member, channels the execution authority directly to a single individual experienced in wind-down phases. His annual compensation for this role was set at $50,000 per year for a period of three years, starting from the engagement letter executed on June 21, 2024.

Finance: draft 13-week cash view by Friday.

eFFECTOR Therapeutics, Inc. (EFTR) - Canvas Business Model: Customer Segments

You're looking at the customer segments for eFFECTOR Therapeutics, Inc. (EFTR) as of late 2025, which is a unique situation given the company announced it would wind down operations in June 2024 and is now trading on the OTCPK market. The 'customers' in this context are less about product sales and more about the stakeholders involved in the wind-down, asset disposition, or potential acquisition of remaining programs.

The primary segments reflect the hierarchy of claims and the strategic interest in the remaining intellectual property, primarily the zotatifin program, following the cessation of active operations.

  • Large pharmaceutical companies seeking late-stage oncology assets.
  • Biotechnology companies looking for novel mechanism of action (MOA) platforms.
  • Secured lender whose repayment is senior to common stockholders.
  • Common stockholders facing potential zero recovery post-liquidation.

The financial reality for the equity holders is stark, reflecting the company's distressed state following the termination of employees and the pursuit of strategic alternatives. As of the end of day on December 5, 2025, the share price was a mere $0.0002.

Here's a quick look at the stakeholders and their relative positions, which defines the current 'customer' dynamic:

Stakeholder Group Key Financial/Statistical Metric (Latest Available) Contextual Data Point
Secured Lender Repayment obligation expected to exceed current available capital. Right to repayment is senior to the rights of the holders of our common stock in any liquidation.
Common Stockholders Share Price as of December 5, 2025: $0.0002. Facing potential zero recovery post-liquidation due to senior debt claims.
Potential Acquirers (Pharma/Biotech) Pre-wind down Employee Count: 11-50. Primary interest is in the remaining clinical-stage candidate, zotatifin, and associated intellectual property.
Short Sellers Short Interest as of October 15, 2025: 5,700 shares sold short. Days to Cover (Short Interest Ratio): 6.3 days based on average trading volume of 4,172 shares.

The segment of large pharmaceutical companies is interested in acquiring the zotatifin program, which has a novel mechanism of action as a selective translation regulator inhibitor (STRI). This interest is what the company was seeking strategic alternatives for, as announced in June 2024. The segment of biotechnology companies might look for platform technology licensing or smaller asset tuck-ins, though the focus remains on the lead oncology asset.

For the common stockholders, the market capitalization based on the December 5, 2025 price of $0.0002 and the implied shares outstanding of approximately 4.70 million (from earlier filings) results in a market capitalization of only $940.00, illustrating the extreme dilution and potential zero recovery scenario. Honestly, the primary 'customer' interaction for the common stockholder now is monitoring the OTCPK trading activity, which showed an extreme projected daily trading range of +/-17,072.54% on December 8, 2025, indicating massive volatility and low liquidity.

The secured lender segment is the most critical counterparty in the wind-down, as their repayment rights take precedence over all equity holders. The company's prior disclosure noted that the lender could declare a default and accelerate repayment obligations, which were expected to exceed the company's available capital at that time. This sets the absolute floor for any potential recovery for the common stockholders, which appears to be zero given the current stock price and operational status.

Finance: review the latest OTCPK trading volume data for EFTR for Q4 2025 to better quantify liquidity risk for the common stockholder segment by Wednesday.

eFFECTOR Therapeutics, Inc. (EFTR) - Canvas Business Model: Cost Structure

You're looking at the cost structure of eFFECTOR Therapeutics, Inc. (EFTR) as it transitioned into a wind-down phase following the June 2024 announcement. The cost base shifted dramatically from clinical-stage operations to liquidation and preservation mode. Honestly, the main costs now are the one-time clean-up charges and the bare-bones overhead to manage the remaining assets and process.

The most immediate, non-recurring cost was tied directly to the workforce reduction. The company expected to incur approximately $600,000 in one-time charges and cash expenditures related to this reduction by June 30, 2024. This covered severance and termination costs for the staff laid off as part of the wind-down decision.

Legal and professional fees represent a significant, ongoing cost category now. These expenses cover the necessary work for pursuing strategic alternatives for the development programs and managing the overall liquidation process. You saw a hint of this trend earlier; for instance, General and Administrative (G&A) expenses in the first quarter of 2024 rose to $3.1 million from $2.9 million the prior year, specifically due to increased legal and consultant fees among other items.

The remaining operational costs are minimal, centered around the governance required to oversee the wind-down. Following the termination of the previous executive team, the board appointed Craig R. Jalbert as the CEO, President, Treasurer, and Secretary, and crucially, the sole member of the board. This structure is designed to keep executive and administrative overhead extremely low, focusing only on fiduciary duties.

The R&D spending, which was the primary cost driver before the wind-down, has been drastically curtailed. To put the reduction in perspective, you need to look at the baseline from the year prior to the wind-down decision.

Here's a quick look at the historical operating expense baseline:

Expense Category Year Ended December 31, 2023 (in thousands) Q1 2024 (in thousands)
Research and Development (R&D) $22,919 $5,300
Sales, General and Admin (G&A) $10,925 $3,100

The $22,919 thousand in Research and Development expenses for the full year 2023 reflects the cost of maintaining clinical programs like tomivosertib and zotatifin. Post-June 2024, this line item effectively collapses to near zero, representing the most significant cost reduction in the entire model.

The current cost structure is dominated by these wind-down activities. You can expect the ongoing cash burn to be primarily:

  • Severance and termination costs already incurred (estimated at $600,000).
  • Ongoing legal and professional fees for strategic review and compliance.
  • Minimal compensation and associated costs for the single-member executive/board role.
  • Costs related to asset disposition or debt management.

Finance: draft 13-week cash view by Friday.

eFFECTOR Therapeutics, Inc. (EFTR) - Canvas Business Model: Revenue Streams

You're looking at the revenue structure for eFFECTOR Therapeutics, Inc. (EFTR) as of late 2025. Honestly, the primary financial reality here is shaped by the June 24, 2024, announcement that the Company terminated employees and would wind down operations, seeking strategic alternatives. This context means the revenue streams are entirely focused on asset monetization rather than ongoing commercial activity.

The core of the expected revenue generation, prior to the wind-down, centered on the pipeline assets, which is now the focus of the strategic alternatives search.

Potential upfront payments or milestones from the Pfizer collaboration

The collaboration with Pfizer involved a preclinical asset, eIF4Ei. The initial terms included an upfront payment. The only concrete figure available related to this partnership is the initial payment received in 2019.

  • Initial upfront payment received from Pfizer: $15.0 million.
  • Subsequent milestone payments for this preclinical asset are contingent upon development progression, which is now subject to the wind-down and strategic alternative review. No specific 2025 milestone achievement is reported.

Proceeds from the sale or licensing of zotatifin and tomivosertib assets

The business model relies on extracting value from the two wholly-owned clinical assets, zotatifin and tomivosertib, through potential out-licensing or sale, especially given the operational wind-down. No realized sale or licensing proceeds for these assets in fiscal year 2025 are publicly available.

Here's a quick look at the assets that represent the potential monetization pool:

Asset Development Status (Pre-Wind Down) Primary Indication Focus
Zotatifin Phase 1/2 clinical trial for solid tumors; ZFA triplet dose escalation ongoing. ER+/HER2- advanced metastatic breast cancer
Tomivosertib Phase 2b KICKSTART trial completed (NSCLC). Acute Myeloid Leukemia (AML) Investigator-Sponsored Trials (ISTs)

Interest income on remaining cash reserves

Interest income is derived from the Company's cash, cash equivalents, and short-term investments held as of the latest reporting period. The cash runway was previously projected into the first quarter of 2025 following a January 2024 financing. Specific cash balances and resulting interest income for the 2025 fiscal year are not available in the latest public disclosures found.

No product sales revenue; the model is purely asset-monetization focused

As a clinical-stage biopharmaceutical company, eFFECTOR Therapeutics, Inc. had no reported product sales revenue in recent historical periods, such as Q4 2023 ($0.0 million). The entire revenue stream structure is built around non-recurring, transactional income from partnerships and asset divestitures.

  • Revenue for the quarter ended December 31, 2023: $0.0 million.
  • Revenue for the quarter ended December 31, 2022: approximately $0.7 million.

Finance: draft 13-week cash view by Friday.


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