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Director Solution Engineering, IQVIA Patient Suite, IQVIA Technologies

This year’s conference highlighted a number of critical areas in clinical R&D including financial management, representation, and eCOA. 

Notable Discussions from SCOPE 2025: Aiming to Calculate, Accommodate, and Innovate for Enhanced Drug Development 

Industry now leveraging reporting system to empower patients and improve research.

   ePROs in Oncology: Breaking Through Barriers for Better Drug Development and Higher Quality Care

Video interview with Sepehr Shojaei, VP, Design Solutions, Lightship

Lightship's Approach to Accessible, Representative, and Impactful Clinical Trials

Lightship prioritizes patient accessibility and centricity in clinical trials, ensuring a seamless and positive experience for every participant. Learn more about:

Lightship's mission and core purpose as a company

How Lightship’s mobile nursing teams and home visits enhance study participation and retention

The role of mobile research units in the community and how they enhance participant education, accessibility, and convenience

Sepehr Shojaei, VP of Design Solutions at Lightship, talks about how the company works with pharma and contract research organization (CRO) partners to support clinical trials that are patient-first and accessible.

Latest Conference Coverage

Lightship’s Approach to Accessible, Representative, and Impactful Clinical Trials

Video interview with David MacMurchy, CEO of Lightship

Accelerate Inclusive Enrollment and Delivery with Lightship

Lightship focuses on patient accessibility and centricity in clinical trials, ensuring the patient experience is a positive one. Learn more about:

Lightship's impact on achieving diversity in clinical trials by engaging underrepresented patient populations

How Lightship utilizes hybrid and decentralized trial designs to reduce patient burden

The impact a patient centric model has on clinical trial participation and outcomes

David MacMurchy, Chief Executive Officer at Lightship, offers some insights into the company's mission toward improving equity and diversity in clinical trials. 

Based on data from the Phase II DAHLIAS (NCT04968912) trial, the FDA has granted Fast Track designation (FTD) to nipocalimab for the treatment of moderate-to-severe Sjögren’s disease.

 The FTD, which is the first ever granted to an FcRn blocker for Sjögren’s disease, will help to advance the development of the investigational therapy, which if approved, would be the first FcRn blocker indicated for the autoantibody-driven disease.

“This marks an additional important step forward in our efforts to bring meaningful advancements to people living with Sjögren’s disease, a serious and debilitating condition,” Katie Abouzahr, MD, vice president, Autoantibody Portfolio and Maternal Fetal Disease Area Leader, Johnson & Johnson Innovative Medicine, said in a press release. “We look forward to continuing to work closely with the FDA to advance the clinical development of nipocalimab and potentially provide a much-needed treatment option for this community.”

Nipocalimab is a high-affinity, fully human, aglycosylated, effectorless, monoclonal antibody, acting as an anti-neonatal Fc receptor (FcRn). In addition to the FTD for Sjögren’s disease, the novel therapy has previously been granted FTD for hemolytic disease of the fetus and newborn (HDFN), warm autoimmune hemolytic anemia, generalized myasthenia gravis (gMG), and fetal neonatal alloimmune thrombocytopenia (FNAIT). Nipocalimab has also been granted Orphan drug designation for warm autoimmune hemolytic anemia, HDFN, gMG, chronic inflammatory demyelinating polyneuropathy, and FNAIT. Additionally, it has been awarded FDA Breakthrough Therapy designation for HDFN and for Sjögren’s disease, with Priority Review status granted for gMG late last year.

The multicenter, randomized, placebo-controlled double-blind, DAHLIAS trial analyzed the efficacy of nipocalimab in patients with primary Sjögren’s disease. The dose-ranging study included 163 patients aged 18-75 years with moderately-to-severely active primary Sjögren’s disease who are seropositive for anti-Ro60 and/or anti-Ro52 IgG antibodies.

Patients were randomly assigned in a 1:1:1 ratio to receive either intravenous nipocalimab at a dose of 5 mg/kg, 15 mg/kg, or placebo every two weeks for 22 weeks, as well as protocol-permitted background standard of care. The trial’s primary endpoint was change from baseline in the Clinical European League Against Rheumatism Sjögren’s Syndrome Disease Activity Index (ClinESSDAI) score at 24 weeks.

The results showed improvements across key measures of disease activity in patients administered nipocalimab. These patients experienced a significant decrease in immunoglobulin G (IgG) of more than 77% with the 15 mg/kg dose level administered every two weeks. Investigators said this reinforces the mechanism of action of nipocalimab through interaction with the neonatal Fc receptor.

Patients administered the 15 mg/kg dose of nipocalimab experienced a significant improvement in the ClinESSDAI score at 24 weeks, showing a greater than 70% relative average improvement in systemic disease activity, which met the trial’s primary endpoint. Nipocalimab also achieved the trial’s key secondary endpoints, including reduced disease activity both systemically and in multiple organ systems, and in improved physician assessments and composite Sjögren’s disease assessments.

Compared with placebo, there were also numerical improvements reported in symptoms identified as most important to participants, which included mouth dryness, eye dryness, vaginal dryness, fatigue, and joint pain.

“The observed reduction in IgG and pivotal autoantibodies, particularly the anti-Ro antibodies, in association with improvement in systemic disease activity and saliva production, represent an exciting advance in our understanding of the disease and how it may be treated effectively,” Ghaith Noaiseh, MD, associate professor, Allergy, Clinical Immunology, and Rheumatology, The University of Kansas Medical Center, said in a press release. “I am also encouraged by the observed trend in many patient-reported measures as they are most important to patients. I look forward to future research to confirm these observations.”

1. Nipocalimab, the first and only investigational treatment to be granted U.S. FDA Breakthrough Therapy designation for the treatment of adults with moderate-to-severe Sjögren’s disease, has now received Fast Track designation. News release. Johnson & Johnson. March 18, 2025. Accessed March 18, 2025. 

https://www.jnj.com/media-center/press-releases/nipocalimab-the-first-and-only-investigational-treatment-to-be-granted-u-s-fda-breakthrough-therapy-designation-for-the-treatment-of-adults-with-moderate-to-severe-sjogrens-disease-has-now-received-fast-track-designation

2. A Study of Nipocalimab in Adults With Primary Sjogren's Syndrome (pSS). ClinicalTrials.gov. Updated March 4, 2025. Accessed March 18, 2025. 

https://clinicaltrials.gov/study/NCT04968912

3. Nipocalimab demonstrates significant clinical improvement in disease activity and IgG reduction in Phase 2 Sjögren’s disease study. News release. Johnson & Johnson. November 14, 2024. Accessed March 18, 2025. 

https://www.jnj.com/media-center/press-releases/nipocalimab-demonstrates-significant-clinical-improvement-in-disease-activity-and-igg-reduction-in-phase-2-sjogrens-disease-study

FDA grants Fast Track designation to Johnson & Johnson’s investigational therapy nipocalimab for the treatment of moderate-to-severe Sjögren’s disease, which could be the first FcRn blocker ever approved for the autoimmune condition.

Phase II DAHLIAS Trial Results Lead to Fast Track Designation for Nipocalimab for Sjögren’s Disease

Join experts from PPD FSP solutions as they discuss the latest FSP trends and opportunities in clinical development, innovative FSP strategies and models, and keys to successfully leveraging an FSP model to drive on-time and on-budget delivery.

https://www.appliedclinicaltrialsonline.com/act_w/fsp-outsourcing-trends


Join experts from PPD FSP solutions—part of the PPD clinical research business of Thermo Fisher Scientific—as they discuss the latest utilization and growth projections of FSP partnerships in the clinical research and development landscape, innovative FSP strategies to address drug development challenges and opportunities, and keys to successfully leveraging an FSP model to drive on-time and on-budget delivery.

Understand the latest utilization and growth projection of FSP partnerships in the clinical research and development landscape

Learn about innovative FSP strategies and models to address drug development challenges and opportunities

Identify the keys to successfully leveraging an FSP model to drive on-time, on-budget delivery


Biopharma and biotech company employees involved in:

Lori Boyce has more than 25 years of experience in the field of clinical research and more than 18 years of experience in clinical operations. She has a broad range of experience working with clients to identify innovative solutions to operational and strategic priorities.



Mike Lydon has more than 16 years of experience within the clinical research industry and has held various leadership roles within the FSP sales and talent resourcing space for top clinical research organizations. His consultative approach to partnerships helps his customers practice innovation, accelerate quality, and reduce burdens.




Webinar Date/Time: Tuesday, April 1, 2025 at 11:00 AM EST

Webcasts: Clinical Operations

Webcasts: CRO/Sponsor

Webcasts: Data Management

Webcasts: Regulatory, Other

FSP Outsourcing Trends and Opportunities

The promise of modern clinical trials is often hindered by a hidden burden: technology that fails to address the realities of clinical research. While science advances with breakthrough therapies and adaptive trial designs, many healthcare stakeholders are constrained by fragmented systems — some outdated, others overly focused on technology without considering the clinical settings or solving the full scope of challenges faced in today’s trials. Wemedoo, a Swiss-based clinical data specialist, is addressing these challenges with 

, redefining the way clinical trials operate.

oomnia has been purposefully designed as a unified solution. Key clinical trial management tools, including EDC, RTMS, eTMF, CTMS, eConsent, ePRO and eSource, are integrative parts of the same solution, eliminating the need for additional integration”, says Dr. Nikola Cihoric, founder of Wemedoo and architect of oomnia.

oomnia: Solving Challenges in Clinical Trials

Sites consistently emphasize the need for user-friendly technology, while sponsors identify study startup delays as a major obstacle to innovation. Fragmented systems worsen these issues by adding complexity and increasing costs, which become even more significant in global studies with dozens of sites and thousands of participants.

oomnia provides an all-in-one solution for clinical trials, removing the need for third-party integrations. When external systems like laboratory information systems or EHRs are necessary, the oomnia eSource module seamlessly connects them, enabling real-time data flow into the research pipeline.

“Sponsors report a 40% faster site activation and up to 50% fewer protocol deviations and data errors in decentralized trials.”

Built on advanced cloud architecture, oomnia ensures consistent performance across studies of any scale, eliminating friction points and enabling real-time management. “In a complex ophthalmology trial with a novel medical device and drug combination, manual queries could be reduced by 66% and a full setup and training completed in only nine weeks’’, emphasizes Dr. Cihoric.

oomnia robust foundation of standardized clinical data forms the cornerstone of its AI capabilities. This strong clinical core ensures AI-driven insights are accurate, clinically relevant, and seamlessly integrated into workflows. By leveraging this solid data framework, oomnia not only delivers impactful AI solutions today but also lays the groundwork to support and advance future AI models in healthcare.

oomnia credibility is reinforced by external validation, including top-tier certifications and inspections, solidifying its status as a trusted leader in clinical trial management. Chosen as the central infrastructure for the Across Global Alliance, encompassing 16 CROs across 60+ countries, oomnia is redefining clinical trial management on a global scale. Dr. Nikola Cihoric, whose clinical experience shaped oomnia development, shares his vision: 'New technologies alone are not enough; we must align them with clinical workflows to truly transform research.”

Driving the Future of Clinical Trials with oomnia

oomnia is built to empower healthcare professionals and streamline clinical trial operations. Standardizing clinical data and seamlessly integrating workflows provide an unmatched foundation for innovation.

oomnia intuitive dashboards tailored to specific roles enable teams across clinical operations, data management, monitoring, risk management, and finance to collaborate effortlessly in real-time.

More than just a tool, oomnia redefines what is possible in clinical trials. The question is not whether you can keep up with the future of healthcare, but whether you are ready to lead it. Let oomnia take you there.

New Era of Clinical Trials with oomnia®: Built for Complexity, Designed for Simplicity 

: ChatGPT usage remains limited to administrative and support work among drug developments professionals; however, a small percentage use it for more advanced tasks, such as predicting pharmacodynamics and tracking adverse events.

: We surveyed 127 drug development professionals between August and October 2023, asking respondents about how they use ChatGPT to support their work. Questions gauged usage levels for support ranging from administrative tasks, such as editing and proofing to more advanced tasks that included generating new chemical structures, identifying new drug targets and novel therapy areas, etc. The survey also asked respondents about their organization’s official stance and outlook on ChatGPT.

: The survey revealed a diverse demographic, with 63% of the respondents being White, and holding doctorate degrees (43%). About half (49%) were employed in pharmaceutical, biopharmaceutical, or contract research organization, while 31% worked in healthcare. Approximately 46% shared that they started using ChatGPT in early 2023. However, organizational attitudes varied, 52% had no formal stance, while 30% encouraged ChatGPT’s integration in the workplace. Usage varied from basic tasks like monthly outlining (39%) to advanced tasks like predicting drug efficacy monthly (less than 10%). Overall, while there's moderate AI familiarity and adoption, organizational attitudes and usage levels of ChatGPT vary widely.

: Most respondents (52%) shared that their organization did not issue a formal stance regarding whether and how ChatGPT should be used, and 81% said that they plan on using ChatGPT to support their work. Approximately 40% of respondents share that they regularly use ChatGPT to carry out supportive tasks, such as creating outlines, editing and organizing written work, and gathering articles. Less than 10% shared that they regularly used ChatGPT to support more advanced work, including generating new chemical structures, predicting pharmacodynamics, and monitoring adverse reactions.

The application of large language modeling (LLM) has exploded over the past two years, most notably with the release of ChatGPT in November 2022. ChatGPT is an LLM developed by OpenAI, an organization whose purpose is to use machine learning algorithms to create human-like responses.

This is accomplished through the processing of large sets of data to respond to user inputs, leading to improvements of its responses through repetitive feedback.

 ChatGPT has been used successfully in a wide range of industries, including education,

In the business space, ChatGPT is gaining momentum where it has the potential to streamline customer service,

 assist in market research,6 and consolidate business decisions.

In medicine, ChatGPT has passed the US medical licensing exam,

 demonstrating the biochemical knowledge equivalent to a third year medical student,

 and has been cited as having the potential to improve clinical workflow.

 However, there are still ongoing limitations to its widespread use within healthcare, stemming from medico-legal complications and harmful or irrelevant results or hallucinations.

Despite these limitations, the potential for ChatGPT’s application in drug development abounds. For example, ChatGPT can not only be used to assist in every day administrative tasks, but can also be used for predicting and explaining drug interactions; converting molecular formulations of compounds to their simplified molecular input line-entry system (SMILES) notation

 and assisting in basic searches for protein data bank files.

Furthermore, ChatGPT can be fine-tuned for even more specific purposes to support drug discovery, such as generating potential chemical structures after being trained on the dataset of drug-like molecules

 or formulating reaction arrays for chemical reactions in high throughput experimentation.

ChatGPT can also simplify the writing process, generate queries for systematic reviews, and help non-native English writers better communicate their scientific ideas.

 Among patients, ChatGPT can be used to assist patient understanding of their medication protocol, potentially improving drug adherence.

 In sum, ChatGPT seems to offer endless possibilities within different realms of drug development.

The US pharmaceutical industry is worth $567 billion in 2022

and disruptive technologies such as ChatGPT are bound to have profound effects within the industry. Understanding the current perceptions and usage of ChatGPT in such a large industry remains critical. However, most of the work currently done on the state of ChatGPT use in the pharmaceutical industry are still theoretical and largely limited to opinion pieces. To our knowledge, this is the first study to quantify the use of ChatGPT within the pharmaceutical industry.

The survey was administered among employees working in drug development in the U.S. (N=127). Survey respondents comprised representatives from at least 45 unique organizations. The survey contained questions designed to assess the integration of ChatGPT (GPT3.5 and/or GPT-4) into respondents' daily job functions and explore associated challenges and barriers. 

ChatGPT usage was assessed using a series of questions about tasks, ranging from administrative tasks such as creating outlines, spell checking, and organizing written work to more sophisticated, tailored usage, such as predicting pharmacokinetics and pharmacodynamics as well as predicting the efficacy and safety of potential drugs. The estimated completion time was approximately 15 minutes. Data collection occurred from August to October 2023. 

All methods were performed in accordance with the relevant guidelines and regulations by including a statement in the methods section to this effect. The study was reviewed by and received exemption status from the Tufts University School of Medicine Institutional Review Board.

The survey was distributed among participants from an internal, proprietary distribution list containing the emails of drug development professionals. Additionally, the survey was shared on Tufts Center for the Study of Drug Development (CSDD)’s social media platforms, specifically LinkedIn and the Tufts CSDD website.

Monetary compensation was not offered for completing the survey. However, participants were provided with the opportunity to vote for their preferred charity from a list of options, which included the American Civil Liberties Union Foundation, Southern Poverty Law Center, The Center for Constitutional, Child Foundation, and Black Mamas Matter Alliance. The charity receiving the highest number of votes was awarded a $300 donation. Respondents also had the option to receive a high-level summary of the study results by providing their email address.

A total of 127 participants completed the survey. The majority identified as White (63%), followed by Asian (21%), multi-racial (7%), Black (5%), and Latino (4%). Half, 50%, identified as men and 46% as women. The mean age was 50 years, and the average work experience was 21 years.

Educational backgrounds varied, with 43% holding a doctorate's degree, 32% a master's degree, 19% a bachelor's degree, 5% a professional degree, 1% an associate degree, and 1% having completed high school. Organizational sizes were distributed as follows: 45% from small-sized organizations, 31% from large-sized organizations, and 24% from mid-sized organizations.

Approximately 50% of respondents were currently employed in pharmaceutical/biopharmaceutical or a contract research organization; 31% of participants worked in an academic medical center, large healthcare system, private clinical trial investigative site, or community-based clinical trial investigative site; and 19% worked in consulting or were solution providers. Additional demographic information is provided in 

Most participants held positions at the manager, senior manager, or director level, comprising 46% of the respondents. Entry level employees accounted for 5% of the respondents. The remaining 49% occupied roles such as C-level executives, owners, senior individual contributors, vice presidents, senior vice presidents, and other positions.

Organizations’ Attitudes Toward ChatGPT

Approximately 52% of respondents shared that their organizations did not provide a formal stance regarding the utilization of ChatGPT. In contrast, 30% of respondents shared that their organizations actively promoted the integration of ChatGPT, while 18% discouraged or prohibited its usage.

Relatedly, when asked about the availability of ChatGPT Plus subscriptions in their workplace, most respondents, 69%, shared that their workplace currently did not provide it and had no plans to do so. When asked about risk management related to ChatGPT, 45% expressed that because they had no intention to use ChatGPT, consequently, they had no plans for risk mitigation.

On the other hand, 17% shared that their organization hired a team of AI specialists tasked with establishing parameters and internal guidelines for its use. Additionally, 10% are offering training to leverage ChatGPT capabilities, while 8% have formed partnerships with OpenAI. See 

Next, among those who said that they are using ChatGPT in their everyday work, we explored for what specific types they were ChatGPT. 

 for a detailed description of the different tasks.

The tasks were categorized into three usage levels, ranging from basic to advanced. Basic tasks included administrative activities such as creating outlines, editing, and proofing reports or manuscripts. Approximately 39% of respondents shared that they used ChatGPT to create outlines for work while 35% shared that they used it for gathering articles and organizing references.

Next, intermediary tasks included slightly more advanced activities such as data management and analysis or explaining novel or difficult concepts. About 39% of respondents shared that they use ChatGPT to help explain difficult to understand concepts; however, less than 20% of respondents shared that they use ChatGPT to handle data.

Lastly, the advanced category contained activities, such as generating new chemical structures and predicting toxic effects of new drugs. Only 14% of respondents shared that they use ChatGPT to identify new drug targets. Less than 10% of respondents shared that they use ChatGPT to assist in the more advanced tasks related to drug development, such as predicting pharmacodynamics, writing code for docking, or monitoring adverse events.

Our study provided baseline ChatGPT usage among drug development organizations to understand whether and how organizations are adopting ChatGPT into daily use. Overall, 52% of organizations represented in our survey did not provide any guidance on the utilization of ChatGPT. Most organizations in our sample—close to 70%—shared that they do not plan on formally implementing ChatGPT. Both results suggest a general hesitancy

 toward using ChatGPT across organizations.

Next, we examined individual’s usage and attitudes towards ChatGPT, which was moderately more favorable to the adoption and usage of ChatGPT. For example, close to 40% of respondents shared that they used ChatGPT to handle basic tasks, such as creating outlines, editing, and organizing written work on a regular or monthly basis. When asked about intermediary tasks, such as analysis, management, storage, and retrieval of data, less than 20% of participants shared that they used ChatGPT for these tasks on a monthly basis.

Next, when asked about more advanced tasks, such as generating new chemical structures or predicting toxic effects of drugs, less than 10% of participants shared that they use ChatGPT to support them in these tasks monthly. Most participants shared that they do not plan on using ChatGPT for more advanced tasks.

What these findings suggest is that most organizations and professionals working in drug development—whether in pharmaceutical sponsor companies or academic research centers—are hesitant about incorporating ChatGPT into their workflow. However, the percentage of those in our sample who regularly use ChatGPT to support their work was higher than the average usage rate among active users of ChatGPT in the general American population, suggesting that those working in the field of drug development may be more comfortable using ChatGPT to support their work.

The study also points to promising potential for future usage in various aspects of drug development, even for the more advanced tasks. For example, identifying new drug targets had the highest level of moderately regular usage—at least a few times a year—among the more advanced tasks.

This finding suggests that although usage of ChatGPT to support robust tasks, such as generating new chemical structures or monitoring adverse drug events, is relatively low compared to less complex tasks, such as editing or performing literature reviews, the potential to scale its usage remains. How drug development companies develop their own datasets for training or create partnerships with OpenAI remain to be seen. Once more robust features are built into ChatGPT and more studies demonstrate its efficacy,

 more drug development professionals may utilize ChatGPT to help them to streamline and perform advanced workflows.

This study has several limitations that should be considered. First, the sample size was relatively small and was only from the United States, which limited the generalizability of the findings. However, data were collected from professionals from biopharmaceutical companies, contract research organizations, and academic institutions. This wide range of industries and views provide a preliminary baseline benchmark of current and future usage of ChatGPT among professionals working in drug development.

Additionally, the study did not evaluate the impact of ChatGPT on actual work outcomes. Future studies may wish to tie different levels of ChatGPT usage to performance metrics—such as study level outcomes; individual work metrics, such as productivity, job satisfaction, and workload—to evaluate its impact on real-world outcomes. Nonetheless, before such studies can be conducted, benchmarks need to be clarified on what constitutes ChatGPT usage in drug development and how AIs will be trained on datasets (i.e. protein data bank files).

In conclusion, the study provided an overview of the baseline usage of ChatGPT among drug development professionals in the United States. While the results from our sample suggest that usage of ChatGPT to support everyday work is still in its infancy, the study also highlights the potential for increased usage of ChatGPT to assist professionals with more advanced tasks.

, Tufts Center for the Study of Drug Development (CSDD), Tufts School of Medicine, Boston, MA USA.

, McGill University, School of Medicine, Montreal, Canada.

1. OpenAI Platform. Accessed May 15, 2024. https://platform.openai.com

2. Baidoo-Anu D, Owusu Ansah L. Education in the Era of Generative Artificial Intelligence (AI): Understanding the Potential Benefits of ChatGPT in Promoting Teaching and Learning. Published online January 25, 2023. doi:10.2139/ssrn.4337484

Despite limitations to its widespread use within healthcare, there is great potential for ChatGPT’s application in drug development.

Melissa Mooney

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