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Analyst

Kripa Devarakonda

Truist Securities · covers Healthcare

Period: Reporting periods mapped to calendar 2024 Q4 – 2026 Q1 (6 quarters).

Questions
11on tracked calls
Challenge rate
9%1 of 11 questions
Companies
4questioned at least once
Reporting periods
6with questions

These figures cover the whole profile: every tracked question, all reporting periods.

How to read these numbers

Challenge rate is the share of questions that pushed back, pressed for specifics or questioned management’s assumptions. It describes how questions were asked on the calls tracked here; it does not measure whether any view turned out to be right.

Rounding. Rates are rounded to whole percentages, so a small share can show as 0% even when some questions were challenging. The count beside each rate is exact; “none of N questions” means no question was challenging.

No questions recorded. “—” means there is nothing to calculate: no questions were recorded for that period on the calls tracked here. It does not mean there was no activity.

Fewer than 3 questions. A company-level rate is withheld when fewer than 3 questions were recorded for that company; the questions are still counted everywhere else.

Small samples. Profiles with fewer than 10 questions are marked Limited sample.

Reporting periods. Questions are grouped by the calendar quarter each company’s fiscal reporting period maps to, not by the date of the call. Periods without a calendar mapping are listed separately under their fiscal label.

Questions asked

Grouped by company, most questions first. Open a company to read its questions, newest reporting period first.

Showing 11 of 11 questions from 4 companies

INCYIncyte5 questions · 5 reporting periods · 0 of 5 challenging
INCY company page →

Calendar 2026 Q1

Can you remind us of data that suggests any synergistic benefit? And given how well ka is entrenched in the myelofibrosis market

Innovation & R&DCompetitive DynamicsTranscript · FY2026 Q1 →
Show response

Pablo cited preclinical additive/synergistic data. Noted Jakafi SVR35 in CALR-mutated patients is only ~20%. 989 fundamentally different: restoring normal hematopoiesis, eliminating malignant megakaryocytes, improving anemia versus Jakafi's symptom-focused approach.

Calendar 2025 Q4

I wanted to just get your expectations for provercitinib in asthma with the phase two readout coming up

Innovation & R&DCompetitive DynamicsTranscript · FY2025 Q4 →
Show response

Bill drew analogy to oral GLP-1 market excitement. Povo positioned for pre-biologic (75% of HS market, ~150K patients on antibiotics/steroids) and post-biologic (50% IL-17/TNF partial responders). Pablo confirmed strong scientific rationale for povo in low-eosinophilic asthma.

Calendar 2025 Q3

is there a rationale to develop both in suboptimal responders as well as in rux naive patients? Or do you see it as a better strategy to focus on one

Innovation & R&DRegulation PolicyTranscript · FY2025 Q3 →
Show response

Pablo confirmed intent to develop 989 across all CALR+ MF populations including naive and post-Jakafi. Will discuss with FDA modified endpoints including potential anemia component. Believes argument exists for modifying traditional SVR35/TSS50 co-primaries.

Calendar 2025 Q2

Can you talk about the patient population where you're seeing increased uptake? And also given the footprint you have established here

Revenue GrowthProduct LaunchTranscript · FY2025 Q2 →
Show response

Mohamed confirmed PV is least penetrated indication driving strong double-digit growth from earlier treatment initiation. Monjuvi showed 59% risk reduction in FL, potential $200M annual revenue by 2028.

Calendar 2024 Q4

Can you talk about the patient population where you're getting uptake and what are the -- what the expectations are in terms of growth?

Revenue GrowthDemandTranscript · FY2024 Q4 →
Show response

Pablo confirmed PV growth driven by earlier treatment supported by MAJIC study data on thrombosis-free survival, plus Medicare copay changes. V617F mutation targets 80-90% of PV cases as next-gen opportunity.

BMYBristol Myers Squibb4 questions · 2 reporting periods · 1 of 4 challenging
BMY company page →

Calendar 2025 Q1

Was there anything in particular that you think might have a significant impact on you know, either the timelines

Show response

Samit confirmed no delays so far, recent HCC and MSI-high CRC approvals came early. Meetings on time, some now in-person. Will engage if timelines change.

Can you talk about expectations from RACE101 in first-line cell lung cancer that's expected later this year

Show response

Samit noted Phase I combined with chemo focusing on safety plus efficacy vs historical controls. Durability is key challenge in SCLC. Data expected H2 2025.

Calendar 2024 Q4

there was an issue with drug availability at average pharmacies is what he said

ChallengingSupply ChainProduct LaunchTranscript · FY2024 Q4 →
Show response

Adam dismissed availability concerns as likely a one-off, confirming teams actively ensuring broad pharmacy distribution across U.S.

with the label change in EU and potentially a change in the U.S. as well. How do you see the peak opportunity now

DemandProduct LaunchTranscript · FY2024 Q4 →
Show response

Adam highlighted steady growth base, ODYSSEY readout in Q2 adding ~1/3 of HCM patients, and REMS easing opening COE capacity.

LLYLilly (Eli)1 question · 1 reporting period · 0 of 1 challenging
LLY company page →

Calendar 2025 Q1

Any update on when we might see data? We've heard the potential to see data in June at a conference

Show response

Dan clarified two Phase II trials: semaglutide combo data to be disclosed first, tirzepatide combo trial of greater interest with timing not yet specified.

PFEPfizer1 question · 1 reporting period · 0 of 1 challenging
PFE company page →

Calendar 2024 Q4

how do you see Pfizer's portfolio in breast cancer evolve over the next few years?

Innovation & R&DCompetitive DynamicsProduct LaunchTranscript · FY2024 Q4 →
Show response

Boshoff outlined CDK4 as potential replacement for all CDK4/6 inhibitors including Ibrance, vepdeg as endocrine backbone replacement, and KAT6 as differentiated epigenetic molecule.

Challenge rate by company

Every company this analyst questioned, most questions first. A company-level rate is shown from 3 questions; below that it is withheld.

CompanyQuestionsChallenge rate
INCY Incyte50%none of 5 questions
BMY Bristol Myers Squibb425%1 of 4 questions
LLY Lilly (Eli)1—Rate withheld: fewer than 3 questions
PFE Pfizer1—Rate withheld: fewer than 3 questions
  • INCY
    Incyte · 5 questions
    0%none of 5 questions
  • BMY
    Bristol Myers Squibb · 4 questions
    25%1 of 4 questions
  • LLY
    Lilly (Eli) · 1 question
    —rate withheld: under 3 questions
  • PFE
    Pfizer · 1 question
    —rate withheld: under 3 questions

Activity by reporting period

Questions recorded for each calendar quarter that companies’ reporting periods map to (not the call date), with the challenge rate for that period. Periods inside the range with no questions are shown as “No questions recorded”.

Questions by calendar reporting period
Calendar periodQuestionsChallenge rateCompanies
2024 Q4425%1 of 4 questions3
2025 Q130%none of 3 questions2
2025 Q210%none of 1 question1
2025 Q310%none of 1 question1
2025 Q410%none of 1 question1
2026 Q110%none of 1 question1
  1. 2024 Q44 questions · challenge rate 25% (1 of 4 questions) · 3 companies
  2. 2025 Q13 questions · challenge rate 0% (none of 3 questions) · 2 companies
  3. 2025 Q21 question · challenge rate 0% (none of 1 question) · 1 company
  4. 2025 Q31 question · challenge rate 0% (none of 1 question) · 1 company
  5. 2025 Q41 question · challenge rate 0% (none of 1 question) · 1 company
  6. 2026 Q11 question · challenge rate 0% (none of 1 question) · 1 company

Topics

Topics tagged on this analyst’s questions.

  • Innovation & R&D6
  • Product Launch4
  • Competitive Dynamics3
  • Regulation Policy2
  • Revenue Growth2
  • Demand2
  • Supply Chain1