TROP-2 ADC in TNBC and HR+/HER2– Breast Cancer

Sector

Biotech

Company

Emerging Biopharma

Therapeutic Area

Oncology

Treatment Modality

Antibody-Drug Conjugate

Product Stage

Clinical

Expertise

Strategy

As an emerging biotech expanded its Phase 1a/b program of a TROP-2 ADC to include triple-negative and HR+/HER2– breast cancer, the communications challenge intensified. While preliminary efficacy data showed promise in both cohorts, the field demanded clarity on differentiation from approved TROP-2 therapies and other late-line competitors.

Situation

As an emerging biotech expanded its Phase 1a/b program of a TROP-2 ADC to include triple-negative and HR+/HER2– breast cancer, the communications challenge intensified. While preliminary efficacy data showed promise in both cohorts, the field demanded clarity on differentiation from approved TROP-2 therapies and other late-line competitors.

Situation

Approach

We built a cross-indication narrative that explained the rationale for cohort expansion and contextualized efficacy and safety data across tumor types. Abstracts, posters, and congress presentations highlighted consistency of activity while acknowledging limitations of early-stage studies. Advisory boards with oncology KOLs were used to refine messaging and stress-test trial positioning.

We built a cross-indication narrative that explained the rationale for cohort expansion and contextualized efficacy and safety data across tumor types. Abstracts, posters, and congress presentations highlighted consistency of activity while acknowledging limitations of early-stage studies. Advisory boards with oncology KOLs were used to refine messaging and stress-test trial positioning.

Approach

Results

Through coordinated publications and congress presence, the company reinforced the scientific relevance of its program in both TNBC and HR+/HER2–. By positioning expansion data transparently, the program built confidence among KOLs while setting expectations for progression into later-phase trials.

Through coordinated publications and congress presence, the company reinforced the scientific relevance of its program in both TNBC and HR+/HER2–. By positioning expansion data transparently, the program built confidence among KOLs while setting expectations for progression into later-phase trials.

Situation

As an emerging biotech expanded its Phase 1a/b program of a TROP-2 ADC to include triple-negative and HR+/HER2– breast cancer, the communications challenge intensified. While preliminary efficacy data showed promise in both cohorts, the field demanded clarity on differentiation from approved TROP-2 therapies and other late-line competitors.

Approach

We built a cross-indication narrative that explained the rationale for cohort expansion and contextualized efficacy and safety data across tumor types. Abstracts, posters, and congress presentations highlighted consistency of activity while acknowledging limitations of early-stage studies. Advisory boards with oncology KOLs were used to refine messaging and stress-test trial positioning.

Results

Through coordinated publications and congress presence, the company reinforced the scientific relevance of its program in both TNBC and HR+/HER2–. By positioning expansion data transparently, the program built confidence among KOLs while setting expectations for progression into later-phase trials.

*Impact studies reflect the collective experience of Biography and its partners.

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Let's Partner

Generating the
Biology Century

We help life sciences teams cut through complexity and move from biology to belief—sharper, faster, leaner.

Let's Partner

Generating the
Biology Century

We help life sciences teams cut through complexity and move from biology to belief—sharper, faster, leaner.