☏ +1 650 501 5505 ✉ [email protected]
Drug Pipeline Review Therapy area: Myelofibrosis40–50 pages · PDF + Excel tracker

Myelofibrosis Drug Pipeline: 51 Assets by Phase

Myelofibrosis pipeline: 51 drug candidates in clinical development, 11 in Phase III, from 31 sponsors. Data as of 3 Oct 2026.

Pipeline Terminal Myelofibrosis Data as of 3 Oct 2026
Candidates in development 51assets Desk-reviewed How this number is madeEvery drug named in an interventional trial, merged across code, generic and brand names, with a live or recent industry trial. Placebo and comparator arms excluded.
Phase III 1122% of pipeline Registry How this number is madeCandidates whose highest phase in a live or recent trial is Phase III (Phase II/III counts as Phase II).
Phase II 816% of pipeline Registry
Phase I 3263% of pipeline Registry
Sponsors 31top 5 hold 47% Registry How this number is madeCompanies credited with at least one candidate: the lead sponsor on most of that candidate's industry trials.
Registered trials 261128 running Registry How this number is madeInterventional trials on ClinicalTrials.gov for the conditions in scope, updated since 3 Oct 2021.
Readouts in 12 months 8Phase II or later Sponsor dates How this number is madeCandidates with a registered primary completion date in the next 12 months. Dates are the sponsor's own and often move.
Trials with US sites 18571% · Europe 33% Registry How this number is madeTrials with at least one site in the United States; Europe is the EU/EEA, the UK and Switzerland. A trial counts in every region where it has a site.

Candidates by highest phase reached

Phase I32
Phase II8
Phase III11

Next registered primary completions, Phase II or later

CandidatePhasePrimary completion
Ropeginterferon Alfa-2BPhase IIDec 2026 (est.)
GivinostatPhase IIDec 2026 (est.)
NavtemadlinPhase IIIDec 2026 (est.)

Candidates in development by lead sponsor

Incyte Corporation10
iOnctura5
Chia Tai Tianqing Pharmaceutical Group Co., Ltd.4
AbbVie3
Bristol-Myers Squibb2

Phase II and III primary completions per quarter

Q4 20263
Q1 20272
Q2 20273
Q3 20270
Q4 20271
Q1 20281
Q2 20283
Q3 20280

Answers at a glance

  • 11 of 51 myelofibrosis candidates (22%) are in Phase III.
  • Incyte Corporation runs the largest myelofibrosis pipeline, with 10 candidates.
  • 8 readouts are due in 12 months; the next is Ropeginterferon Alfa-2B in Dec 2026.
  • 72 trials are recruiting patients now; 71% of all trials have a US site and 33% a European one.
51 candidates261 trials58 countriesData as of 3 Oct 2026Next refresh by 1 Jan 2027
USD 3,000Pipeline Snapshot Download Free Sample Request the Review
Edition: data as of 3 Oct 2026 Next refresh: by 1 Jan 2027 Change: First edition

Request a free sample

A sample of the Myelofibrosis Pipeline Review: the full chapter list, the tracker columns and two asset profiles from the report. The Research Desk reviews your request and emails it, usually within one business day.

Myelofibrosis has 51 drug candidates in active clinical development, of which 11 are in Phase III, 8 in Phase II and 32 in Phase I, according to Douglas Insights' count of 261 interventional trials registered on ClinicalTrials.gov (data as of 3 Oct 2026).

The myelofibrosis drug pipeline is the set of medicines that sponsors are still testing in people for this condition: each candidate is counted once, at the highest phase it has reached in a running or recently completed trial. Medicines already on the market and studied only in Phase IV trials are kept out of the count.

How many myelofibrosis drugs are in each phase of development?

Douglas Insights counts 11 myelofibrosis candidates in Phase III, 22% of the 51 assets in development; Phase II holds 8 and Phase I holds 32.

Phase I32Phase II8Phase III11
Candidates by highest phase reached. Source: Douglas Insights from ClinicalTrials.gov, data as of 3 Oct 2026.
Phase (highest reached)AssetsShare of pipeline
Phase III1122%
Phase II816%
Phase I3263%
Total51100%

Phase I/II candidates sit in the Phase I row and Phase II/III candidates in the Phase II row, so each myelofibrosis asset appears in exactly one row. The 128 trials still recruiting or running carry 49% of the 261 registered trials in scope.

Which approved myelofibrosis medicines are still in trials?

2 medicines already on the market are still being tested in myelofibrosis Phase IV trials; Ruxolitinib has the most, with 81 registered trials.

MedicineLead sponsorRegistered trials
RuxolitinibSeveral sponsors81
MomelotinibSierra Oncology LLC - a GSK company13

Post-approval myelofibrosis trials test new doses, new patient groups and head-to-head comparisons. They set the standard of care that every candidate in development will be measured against, so the paid review profiles each one.

How many myelofibrosis trials are recruiting patients now?

72 myelofibrosis trials are recruiting patients and 9 more have not started recruiting yet, out of 261 interventional trials in scope; together they make up 31% of the trial base.

Registry statusTrialsShare
Completed8031%
Recruiting7228%
Active, not recruiting4718%
Terminated3313%
Status not verified124.6%
Not yet recruiting93.4%
Withdrawn83.1%

Terminated, suspended and withdrawn myelofibrosis trials stay in the trial base so that a stalled programme is visible, but a candidate whose only trials stopped is no longer counted as in development.

Which companies lead the myelofibrosis pipeline?

Incyte Corporation leads the myelofibrosis pipeline with 10 candidates; the top 5 sponsors hold 47% of the 51 assets, and 31 sponsors run at least one.

SponsorAssets in developmentShare
Incyte Corporation1020%
iOnctura59.8%
Chia Tai Tianqing Pharmaceutical Group Co., Ltd.47.8%
AbbVie35.9%
Bristol-Myers Squibb23.9%

Industry sponsors lead 133 of the 261 myelofibrosis trials (51%); universities, hospitals and public funders lead the rest. A sponsor is credited with an asset when it is the lead sponsor on most of that asset's industry trials.

Which drug types and mechanisms dominate the myelofibrosis pipeline?

Mechanism and drug-type classification for the 51 myelofibrosis candidates is done by the research desk asset by asset, each with a cited source, and is published in the paid review together with the white-space map.

What myelofibrosis trial readouts are coming next?

8 myelofibrosis candidates in Phase II or later have a registered primary completion date in the next 12 months; the next three are below, each linked to its registry record.

CandidateSponsorPhasePrimary completionRegistry
Ropeginterferon Alfa-2BPharmaEssentiaPhase IIDec 2026 (estimated)NCT06770842
GivinostatItalfarmacoPhase IIDec 2026 (estimated)NCT01761968
NavtemadlinKartos Therapeutics, Inc.Phase IIIDec 2026 (estimated)NCT06479135

Primary completion is the date a sponsor expects the last patient to finish the main measurement, so data usually follow within months. Dates marked estimated are the sponsor's own forecast on the registry and often move.

How many myelofibrosis readouts fall in each quarter?

13 myelofibrosis candidates in Phase II or later reach registered primary completion over the next eight quarters, with the most, 3, due in Q4 2026.

QuarterPhase III readoutsPhase II readoutsTotal
Q4 2026123
Q1 2027022
Q2 2027033
Q3 2027000
Q4 2027101
Q1 2028011
Q2 2028213
Q3 2028000

Each candidate is counted once, at its next readout. The paid catalyst calendar names every readout with its trial, sponsor and design, adds filings and regulatory decisions, and runs 24 months ahead.

Which countries host the most myelofibrosis trials?

United States hosts the most myelofibrosis trials, with sites in 185 of the 261 studies (71%); trials in scope run in 58 countries in all.

CountryTrials with a siteShare of trials
United States18571%
Italy6224%
France5320%
Germany5220%
United Kingdom4818%
Spain4618%
Australia4216%
Canada3915%

A multinational myelofibrosis trial is counted once in every country where it has a site, so the shares add up to more than 100%. Country spread shows where sponsors are building the evidence that regulators in each market will ask for.

Where are myelofibrosis drugs being tested?

185 of the 261 myelofibrosis trials (71%) have a site in the United States, 86 (33%) in Europe and 37 (14%) in China; 37 of the 51 candidates in development are tested in the US.

RegionTrials with a siteShare of trialsCandidates testedRegulator
United States18571%37FDA
Europe (EU/EEA, UK, Switzerland)8633%34EMA, MHRA, Swissmedic
China3714%14NMPA
Japan238.8%15PMDA
Rest of world7328%30national regulators

Each region's trials are the evidence its regulator will review: the FDA in the United States, the EMA (with the MHRA and Swissmedic) in Europe, the NMPA in China and the PMDA in Japan. A multinational myelofibrosis trial counts once in every region where it has a site, so the shares add up to more than 100%. A candidate tested only outside the US and Europe is often a licensing opportunity for sponsors in those markets.

What has changed in the myelofibrosis pipeline since the last update?

This is the first edition of the myelofibrosis pipeline count, dated 3 Oct 2026. The next refresh is due by 1 Jan 2027, and each refresh lists the assets that entered, advanced or dropped out.

How does Douglas Insights count the myelofibrosis pipeline?

Douglas Insights read 261 interventional trials registered on ClinicalTrials.gov for the conditions "Primary Myelofibrosis", "Myelofibrosis" and updated since 3 Oct 2021, then grouped every drug or biologic named in them into 51 unique candidates.

  1. Code names, generic names and brand names of the same molecule are merged into one candidate, and every merge is reviewed by the research desk.
  2. A candidate counts when it has a trial that is recruiting, running, or completed in the last 24 months, and at least one industry-sponsored trial.
  3. Its phase is the highest phase among those trials; placebo, standard-of-care and comparator arms are not candidates.
  4. Each figure on this page is drawn from one frozen dataset that passes ten checks before release, and the owner approves every edition.

Read the full approach on the research methodology page, or browse other Pharmaceuticals research.

What does the Myelofibrosis Pipeline Review include?

The Myelofibrosis Pipeline Review covers all 51 candidates in an Excel tracker and profiles the leading 25 in a 40–50 page report, ending with the research desk's ranked view of the candidates most likely to win.

11 chapters40–50 pages25 asset profilesExcel tracker of all 51 candidates
01Executive summary and our call2–3 pp

The pipeline on one page and the desk's verdict on where myelofibrosis treatment is heading.

  • Pipeline size and phase mix
  • The three calls that matter
  • What changed since the last edition
02Disease and unmet need3 pp

Who is treated today, what current therapy leaves unmet, and how regulators judge new medicines.

  • Patient population and diagnosis
  • Treatment guidelines and gaps
  • Regulatory endpoints
03Approved therapies3 pp

The marketed medicines every myelofibrosis candidate will be measured against.

  • Marketed medicines and their sponsors
  • Post-approval trials
  • The bar a new entrant must clear
04Pipeline at a glance4 pp

Every candidate counted by phase, drug type, sponsor and country.

  • Assets by phase and drug type
  • Sponsors by size of pipeline
  • Trial footprint: US, Europe, China, Japan
05Mechanism landscape and white space5 pp

Which mechanisms are crowded and which no sponsor has entered.

  • Mechanism classes and crowding
  • Classes with no candidate yet
  • Differentiation by route and dosing
06Key asset profiles12–15 pp

The leading 25 candidates, one profile each, every claim linked to a source document.

  • Design and endpoints of the pivotal trials
  • Data to date, with sources
  • Next readout and the risk to it
07Catalyst calendar3 pp

Readouts, filings and regulatory decisions 24 months ahead.

  • Readouts by quarter
  • Filings and regulatory decisions
  • Date confidence for each event
08Deals and partnering3 pp

Who is licensing, buying and partnering in myelofibrosis, and on what terms.

  • Licensing and M&A in the area
  • Deal terms where disclosed
  • Sponsors open to partnering
09Sponsor landscape3 pp

Large pharma against biotech, and how concentrated the pipeline is.

  • Pipeline share by sponsor
  • Sponsor-by-phase matrix
  • New entrants since the last edition
10Our call: winners, risks, opportunities3–4 pp

The candidates most likely to win, ranked, with the reasoning and evidence.

  • Ranked candidates
  • Risks that could change the order
  • Openings for new entrants and investors
11Methodology and source log2 pp

How the count is built and every document behind it.

  • How candidates are counted and merged
  • Every source document listed
  • The ten quality checks

Ways to buy the Myelofibrosis review

OptionWhat you getDeliveryPrice
Pipeline SnapshotThis therapy area as published: PDF report + Excel trackerReady nowUSD 3,000Enquire
Pipeline ReviewYour indication, geography and phase cut-off; ranked calls and an analyst call2–3 weeksFrom USD 4,000Enquire
Company AssessmentOne sponsor's full pipeline against its peers2 weeksFrom USD 5,000Enquire

Email me the sample and chapter listAsk for a quote

Frequently asked questions about the myelofibrosis pipeline

How many drugs are in the myelofibrosis pipeline?

51 drug candidates are in active clinical development for myelofibrosis, with 11 in Phase III, per Douglas Insights (data as of 3 Oct 2026).

Which company has the most myelofibrosis drugs in development?

10 candidates make Incyte Corporation the largest myelofibrosis pipeline sponsor, out of 31 sponsors counted by Douglas Insights.

When is the next myelofibrosis trial readout?

Dec 2026 is the registered primary completion of the Phase II trial of Ropeginterferon Alfa-2B (NCT06770842), the next myelofibrosis catalyst in Douglas Insights' calendar.

How many myelofibrosis trials run in the United States and Europe?

185 myelofibrosis trials have a US site and 86 a European site, out of 261 registered trials counted by Douglas Insights (data as of 3 Oct 2026).

How often is the myelofibrosis pipeline count updated?

90 days is the refresh cycle; this edition uses registry data as of 3 Oct 2026 and the next is due by 1 Jan 2027.

Research & citation

This review was researched, written and reviewed by the Douglas Insights Research Desk under the Douglas Insights editorial standards. Material errors are logged in the corrections log. No section is sponsored.

Cite this page Douglas Insights (2026). Myelofibrosis Drug Pipeline, data as of 3 Oct 2026. https://www.douglasinsights.com/pipeline/myelofibrosis/