Article

Closing the readiness gap for CGTs in community-based care

Cell and gene therapies (CGTs) are no longer just a scientific breakthrough — they are becoming a core commercial priority for many biopharma companies. These therapies have the potential to deliver durable and, in some cases, curative outcomes by targeting the underlying genetic or cellular causes of disease.  

But to achieve that promise at scale, commercial strategy and product access need to evolve alongside the science. Many biopharma companies describe a common gap: although eligible patients may benefit from these therapies, access remains limited. Per McKinsey, only one out of five eligible patients is ultimately treated1

Several factors contribute to limiting access to CGTs, including high upfront costs2 and meeting strict utilization management protocols from payers3. In addition, geographic and logistical constraints are also major contributors since these complex therapies often require specialized facilities and handling that are limited to a few academic medical centers4

To reduce these geographical and logistical limitations to product access, it’s critical to expand into the community hospital setting. But that expansion requires addressing significant barriers. 

The next phase of CGT access  

For many CGTs today, a small number of academic medical centers remain the primary path to treatment. These centers play a critical role in the early phases of adoption. They have the infrastructure, specialized staff, and experience needed to support highly controlled rollout models. 

But that model alone may not be enough going forward. 

Biopharma companies are increasingly focused on expanding access beyond these few early-adopter environments and into the many hospitals in community settings. If CGTs are to reach more patients, care delivery must extend closer to where many patients already receive treatment.  

For example, oncology patients often begin their treatment journey with a community oncologist. By the time they are eligible for a cell therapy, they may have already gone through multiple lines of treatment. They may be clinically vulnerable, financially strained, and reluctant to travel far from home for care. 

There is also a capacity issue. Academic medical centers alone may not be able to absorb the level of patient volume many manufacturers expect as more therapies move toward launch and broader adoption. Expanding CGTs to non-academic health systems and community sites of care is becoming a commercial necessity.

Scientific readiness surpasses operational readiness 


Unfortunately, cell and gene therapies are advancing faster than the delivery models needed to support them in broader care settings. That gap is especially visible in community hospitals, where operational processes may still be lagging, financially risky, or difficult to scale for CGTs. Even when hospitals are clinically motivated to participate, activation can stall when teams have to coordinate staff training, referral workflows, reimbursement, product handling, chain-of-custody documentation, and patient scheduling.  

As a result, biopharma companies may find that only a limited number of community sites are truly launch-ready. If these barriers are not addressed, the impact can be significant and result in: 

  • Slower launch uptake 
  • Inconsistent product access 
  • Greater strain on health system partners 
  • More difficulty sustaining long-term adoption 


Common barriers to community-based CGT expansion 


Based on what our partners are seeing in the market, several barriers stand out. 

1. Onboarding can take longer than teams expect 

Standing up new community sites for a CGT often requires far more than clinical alignment. Operational execution can become a bottleneck. Biopharma companies and hospitals may need to work through: 

  • Contracting and terms and conditions 
  • Credit checks and credit limit decisions 
  • Internal workflow setup 
  • Staff education and cross-functional coordination 

These steps can take months. The challenge is often greater for emerging biopharma companies launching a CGT for the first time. Many do not yet have the internal playbooks, staffing models, or launch infrastructure that could expedite site onboarding. At the same time, many community hospitals lack CGT-specific operational experience. Without a clearer path to activation, site expansion can stall before treatment even begins. 

“Many community hospitals are highly capable care settings, but they may not yet have cell and gene therapy-specific operational experience. That is why successful expansion depends on creating a clearer path to readiness — one that helps teams navigate requirements, reduce friction, and build confidence across stakeholders.”

Ryan Telford, PharmD
Vice President, Health System Pharmacy Portfolio Strategy
Cencora


2. Financial exposure is real for community hospitals

Financial risk is another major factor. CGTs carry a high upfront cost, and hospitals may face significant exposure when therapy is purchased, delivered, or staged before final access or administration is complete. If scheduling delays, product access issues arise or logistics disruptions occur, expensive inventory may remain on site longer than expected.

That creates real balance-sheet pressure for health systems. For hospitals in community settings, that risk can be enough to slow or limit program participation — even when there is clinical interest and patient need.

Biopharma companies looking to expand their footprint need to think beyond product distribution alone. They should consider models that reduce the financial burden on hospital partners and create a more workable path to adoption.

3. The patient and caregiver experience can become a barrier of its own

Even when a community site is operationally enabled, the patient journey can still be difficult to navigate. Being treated with a CGT often involves complex logistics and ongoing coordination, which can become burdensome if the orchestration of services and staff is fragmented. In many cases, patients and caregivers absorb a large share of these burdens themselves, dealing with: 

  • Scheduling delays 
  • Administrative complexity 
  • Coordination across multiple stakeholders 
  • Post-infusion support and monitoring needs 

For some therapies, caregivers may need to be available around the clock for a defined period after infusion. Not every patient has that level of support.  

These realities can delay therapy initiation. In some cases, they may discourage patients from moving forward at all. For manufacturers, that means access to these therapies is not just about site activation. It is also about reducing friction across the treatment journey. 

What this means for CGT launch teams 


The gap between scientific ambition and real-world execution is widening. CGT pipelines are accelerating. At the same time, health systems are managing operational, financial, and patient-related friction that can make expansion difficult — especially outside major academic centers. 

For commercial leaders, the implication is clear: if manufacturers do not find ways to support adoption in hospitals and community settings, they may struggle to reach the patient volumes needed to achieve both market potential and patient impact. Launch planning should account for the realities of community expansion earlier, more deliberately, and with the right operational support in place. 

A more connected model for launch readiness 


Biopharma companies preparing for commercial launch often need more than strategic advice alone. They need partners with proven experience connecting access, distribution, site readiness, and patient coordination at scale. As CGTs move into their next commercial phase, success will depend not only on the strength of the therapy but also on the strength of the systems that support it. 

Cencora works across the healthcare ecosystem, with relationships spanning CGT manufacturers and provider networks, including community care providers. That vantage point provides visibility into the pressures that launch teams and sites of care are navigating as they work to responsibly expand product access. 

Contact our team to learn how Cencora can help address the operational, financial, and product access challenges shaping CGT launch success. 

Connect with our cell and gene experts

Schedule some time with our cell and gene experts today. We look forward to hearing from you.
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Sources:

  1. Furstenthal, L. Steadfast but nimble: CEO Christi Shaw on cancer treatment’s cutting edge. McKinsey & Company. 26 January 2023. Accessed 20 May 2026. Available online at: https://www.mckinsey.com/industries/life-sciences/our-insights/steadfast-but-nimble-ceo-christi-shaw-on-cancer-treatments-cutting-edge

  1. Berry, D. at al. Ensuring patient access to gene therapies for rare diseases: Navigating reimbursement and coverage challengesAmerican Society of Cell and Gene Therapy. 29 January 2025. Accessed 11 June 2026. Available online at: https://www.asgct.org/advocacy/policy-statements/ensuring-patient-access-to-gene-therapies-for-rare-diseases-navigating-reimbursement-and-coverage-challenges

  1. American Society of Cell and Gene Therapy. Community Quick Takes: Access to Approved Cell and Gene Therapies11 April 2025. Accessed 11 June 2026. Available online at: https://www.youtube.com/watch?v=jXV8KkBFpkA&t=18s

  1. Nze, C. et al. Barriers to accessing cellular therapy for patients receiving care in community practicesHematology.8 December 2023. Accessed 11 June 2026. Available online at: https://pmc.ncbi.nlm.nih.gov/articles/PMC10727008/


This article may 
contain marketing statements and shall not constitute legal advice. Cencora, Inc. strongly encourages readers to review all available information related to the topics mentioned herein and to rely on their own experience and expertise in making decisions related thereto.

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