RMC-6236-001: what clinicians are saying
daraxonrasib (RMC-6236) in RAS-mutant advanced solid tumors · NCT05379985 ↗ · Phase 1/Phase 2 · Revolution Medicines, Inc.
RMC-6236-001 examines RMC-6236 safety in advanced solid tumors with specific RAS mutations; discussion of non-small cell lung cancer (NSCLC) combines support for activity beyond G12C with questions about the highlighted response estimate. The report cites 19 physicians, including 15 medical oncologists, and a contributor described in the source as involved in the trial. Further questions concern lower NSCLC dosing and whether previously treated pancreatic ductal adenocarcinoma activity warrants practice change. How can teams explain cohort-specific benefit estimates and toxicity burden while separating evidence from access?
- v1.0.0 · edition 1
- commentary checked Nov 4, 2026 UTC
- Standard
- 47 from 19 confirmed clinicians
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9 findings, and what sits behind each
01. Speakers welcome NSCLC activity beyond G12C; one discussion challenges the highlighted 42% response estimate
23 statements · 23 passages · 7 sources · 5 speakers named (any role)
Limitations recorded: 4. Feeds the Medical Affairs question.
Draws on: Secondary endpoints, Design and conduct, The comparison, Population and setting.
02. Speakers favor a lower NSCLC dose on tolerability grounds and stress the burden of toxicity
30 statements · 31 passages · 9 sources · 6 speakers named (any role)
Limitations recorded: 4. Feeds the Medical Affairs question.
Draws on: Primary endpoint: Incidence and severity of treatment-emergent Adverse Events (AEs) and serious AEs, including incidence and severity of findings in laboratory values and vital signs, Safety and tolerability, Population and setting, The comparison.
03. Speakers differ on whether previously treated PDAC activity is enough to change practice
36 statements · 27 passages · 16 sources · 20 speakers named (any role)
Limitations recorded: 4. Feeds the Medical Affairs question.
Draws on: Secondary endpoints, The comparison, Population and setting, Design and conduct, Primary endpoint: Incidence and severity of treatment-emergent Adverse Events (AEs) and serious AEs, including incidence and severity of findings in laboratory values and vital signs, Safety and tolerability.
04. Speakers describe manageable PDAC toxicity as work-intensive; one clinician asks whether skin toxicity is unfamiliar
12 statements · 11 passages · 7 sources · 8 speakers named (any role)
Limitations recorded: 3. Feeds the Medical Affairs question.
Draws on: Safety and tolerability, Primary endpoint: Incidence and severity of treatment-emergent Adverse Events (AEs) and serious AEs, including incidence and severity of findings in laboratory values and vital signs.
05. Speakers see a conceptual advance and discuss a possible RAS-treatment platform
18 statements · 21 passages · 11 sources · 9 speakers named (any role)
Limitations recorded: 4. Feeds the Medical Affairs question.
Draws on: Population and setting, Safety and tolerability.
06. Speakers flag resistance and sequencing gaps; one also highlights CNS activity
14 statements · 15 passages · 7 sources · 5 speakers named (any role)
Limitations recorded: 4. Feeds the Medical Affairs question.
Draws on: Population and setting, Secondary endpoints.
07. Speakers welcome first-line PDAC monotherapy, while combination views range from enthusiasm to doubt
16 statements · 15 passages · 9 sources · 9 speakers named (any role)
Limitations recorded: 5. Feeds the Medical Affairs question.
Draws on: Secondary endpoints, The comparison, Population and setting.
08. One clinician asks about off-label NSCLC access; other sources stress route-specific restrictions
15 statements · 16 passages · 10 sources · 6 speakers named (any role)
Limitations recorded: 5. Feeds the Medical Affairs question.
Draws on: Population and setting.
09. How do account-authored assessments frame daraxonrasib activity and severe adverse events in NSCLC and PDAC?
2 statements · 2 passages · 2 sources · 2 speakers named (any role)
Limitations recorded: 2. Feeds the Medical Affairs question.
Draws on: Primary endpoint: Incidence and severity of treatment-emergent Adverse Events (AEs) and serious AEs, including incidence and severity of findings in laboratory values and vital signs, Secondary endpoints.
Counts overlap, since one statement can back several findings. They show what the report kept, not how many clinicians agree. The full report includes the interpretations and source links.
Select a finding to see what the full report holds for it: how many verified statements and of what kind, the passages behind them, the sources and speakers, and the limits it records. Speakers named counts every name a finding's statements carry, of any role and including names not yet matched to a person, so it is not the report's count of cited voices or confirmed clinicians and can be larger. Select a part of the trial to see which findings draw on it.
- Finding 1 of 9
Speakers welcome NSCLC activity beyond G12C; one discussion challenges the highlighted 42% response estimate
- statements
- 23
- passages
- 23
- sources
- 7
- speakers named, any role
- 5
What the statements areViews 12Questions and uncertainty 3Clinical experience 0Comparisons 2Restated results and context 6Statement-to-passage links (a passage can back several statements)Supporting a statement 25Giving context 1Recorded with the finding- Limitations: 4
- Feeds the Medical Affairs question
- 6 posts and articles
- 1 podcast or video
Draws on: Secondary endpoints, Design and conduct, The comparison, Population and setting.
In the full report: the interpretation in full, all 23 statements cited to source and date, and the 7 sources linked where public.
Thicker lines mean more shared statements. A finding without a line goes beyond the registered design. Counts overlap, since one statement can back several findings, and they show what the report kept, not how many clinicians agree.
Abbreviations AE, adverse event; CNS, central nervous system; CRC, colorectal cancer; DLT, dose-limiting toxicity; HCP, healthcare professional; MCP, Model Context Protocol, how AI agents read the report; NPI, National Provider Identifier, the US registry number for clinicians; NSCLC, non-small cell lung cancer; PDAC, pancreatic ductal adenocarcinoma.
The full RMC-6236-001 report gives each finding its interpretation, the attributed views behind it, counterviews, limits and the verified statements, each linked to the original. One report in the catalog, IDeate-Lung01, is free in full, so you can see what a paid report holds before you buy: read the free IDeate-Lung01 report.
How can Medical Affairs preserve cohort-specific benefit estimates, the practical burden of toxicity and the distinction between evidence and access in the same conversation?
Raised by the leading finding. The report shows what clinicians said and the sources behind it; it does not settle the question.
By the numbers
free- 87commentary sources screened
- 50sources cited by verified statements
- 34named in screened sources
- 34voices cited in the report
- 29cited voices with a verified identity
19 cited clinicians, voices with a confirmed clinical role, of them 19 physicians. By role and specialty:
- 15 physician, Medical oncology
- 2 physician
- 1 physician, Cardiology
- 1 physician, Pathology
A verified identity says who a voice is. A cited clinician also has a clinical role confirmed by the NPI registry or their own institution's staff page. Verified voices without such a role, such as researchers, advocates, company staff, or clinicians whose role only a source or their own profile states, are not counted as clinicians.
Also in the sources: 11 organizational or shared accounts, not counted as people.
- 196verified statements, each linked to its source
- 47of them from speakers with a confirmed clinical role
- 9findings
Built by AI from public clinician commentary, checked by automated review; every statement links to its source.
Screened sources were retrieved for this trial. Cited sources back at least one verified statement and include primary sources used for context. No count estimates how many clinicians hold a view. Size (Standard · 196 verified statements · 47 from 19 confirmed clinicians) is set by the verified statements. Standard and Deep need at least 5 confirmed clinicians cited (role verified by the NPI registry or their own institution's staff page); with fewer, a report is sold one size down. Statements from sponsors, hosts and organisations are labelled and count apart from identified clinicians. A confirmed clinical role is one verified by the NPI registry or by the person's own institution's staff page; a role a source only states is not counted. In the summary, clinicians are the cited voices with a confirmed clinical role, physicians are those whose confirmed role is a physician's (not physician assistants, nurses or pharmacists), and each specialty count is a role and specialty row under People.
What's inside
free| Section | Items | Access |
|---|---|---|
| Findings with interpretation, counterviews and limits | 9 | Titles free |
| Detailed analysis | 9 sections | Paid |
| Verified statements with short source quotes and links | 196 | Paid |
| Who said each statement, with each cited voice's role and what confirmed it (NPI registry or staff page) | 34 | Every edition |
| Trial aspects mapped | 13 | Free |
| Sources with links | 50 | Counts free |
| MCP access for your AI agent, same license key | Included | Every edition |
| Verified speaker IDs as data (NPI, social and scholarly IDs) | 29 | 12-month plan add-on |
Every edition, the free report included, names who said each statement, as the source shows them. Each named voice's card gives a clinical role only when the NPI registry or the person's own institution's staff page confirms it, and says which; a role only a source states is labelled as the source's. Here 19 of the 34 cited voices have a role confirmed that way. Every edition also comes with MCP access, so your AI agent reads the same evidence with your license key. The verified speaker identities add-on, sold with 12-month plans, adds each verified person's IDs as data (the NPI number, X, Bluesky and LinkedIn accounts, ORCID and institutional pages), so your team can check each attribution itself. It is for checking attribution inside your organization, never for outreach or targeting, and it does not unlock who said what.
Trial aspects
12 discussed · 1 no commentary found · 0 assessment incomplete| Aspect | Statements | Sources |
|---|---|---|
| Primary endpoint: Incidence and severity of treatment-emergent Adverse Events (AEs) and serious AEs, including incidence and severity of findings in laboratory values and vital signs | 15 | 10 |
| Primary endpoint: Number of Participants with Dose-Limiting Toxicity (DLT)no commentary found | 0 | 0 |
| Secondary endpoints | 24 | 19 |
| Population and setting | 18 | 11 |
| The comparisonThe registered arms and what clinicians said about how they compare. | 14 | 11 |
| Safety and tolerability | 23 | 9 |
| Design and conduct | 13 | 4 |
| Dose optimization and the efficacy–tolerability trade-off | 11 | 7 |
| Broader RAS coverage, biological relevance and platform interpretations | 15 | 10 |
| ctDNA, resistance, prior RAS-inhibitor sequencing and CNS questions | 11 | 6 |
| First-line PDAC monotherapy and distinct combination strategies | 14 | 8 |
| Access, eligibility, patient support and indication-specific communication | 15 | 10 |
| Historical benchmarks, randomized corroboration and thresholds for practice change | 29 | 14 |
Discussed means at least one verified statement addresses the aspect, not that every question in it is covered: gaps inside a discussed aspect are listed under Scope and limits, and the full report gives each aspect its own limitations. No commentary found means none in the sources read. Assessment incomplete marks an aspect with no statement found while known source limits apply.
Sources
free| Channel | Screened | Cited | |
|---|---|---|---|
| X threads | 75 | 39 | |
| Bluesky threads | 5 | 3 | |
| LinkedIn posts | 4 | 4 | |
| YouTube | 3 | 3 | |
| Primary sources, cited for context, not screened | |||
| Publications | not screened | 1 | |
max 33 / quarter
- Screened window
- Nov 11, 2022 → Oct 7, 2026
- Cited window
- Nov 11, 2022 → Sep 14, 2026
- Retrieved
- Nov 4, 2026
The trial
from ClinicalTrials.gov- Title
- A Multicenter Open-Label Study of RMC-6236 in Patients With Advanced Solid Tumors Harboring Specific Mutations in RAS
- Registry
- NCT05379985
- Study IDs
- RMC-6236-001
- Sponsor
- Revolution Medicines, Inc.
- Design
- Phase 1/Phase 2 · Interventional, single group
- Status
- Recruiting
- Enrollment
- 754 estimated
- Registered
- 2022-05-18
- Start
- 2022-05-31 actual
- Primary completion
- 2027-05-31 estimated
- Primary endpoint
- Incidence and severity of treatment-emergent Adverse Events (AEs) and serious AEs, including incidence and severity of findings in laboratory values and vital signs
- Interventions
- 1 registered
Scope and limits
freeThis report does not judge efficacy, estimate HCP prevalence or consensus or give treatment advice.
- Discussion that does not name the trial may be missing from this edition.
- Not yet captured in this edition: a view on treatment-history uncertainty in commentary about RAS-targeted therapy for progressive pancreatic cancer.
- Not yet captured in this edition: a remark on biomarker-defined combination-trial options and geographic access for patients with non-small cell lung cancer.
- Not yet captured in this edition: a view on first-line daraxonrasib plus chemotherapy in RAS-mutant metastatic pancreatic cancer.
- Not yet captured in this edition: a view on testing chemotherapy-free treatment against standard care in frontline pancreatic cancer.
- Not yet captured in this edition: a view on chemotherapy-free treatment versus standard care in frontline pancreatic cancer.
- Not yet captured in this edition: a view on the value of treatment response specifically for patients who respond.
- 79 passages in 48 sources used in this report were not fully assessed for clinician views, so a view there may be missing from this edition.
- 57 statements in the sources reviewed for this edition are about other patients or topics, or only mention the trial, and are not counted.
- Further source limits: discussion that describes the trial without naming it may be incomplete; some discussion that describes the trial without naming it may be missing; 100 sources about other trials or topics are not included; 398 sources that may describe the trial without naming it were not read.
- This report describes the sources reviewed for this edition, not all HCPs or all public discussion. Some potentially relevant sources were not read, and some passages were not fully assessed; unnamed trial references may also have been missed.
- Repeated cross-platform posts, reposts, organizational summaries and relayed presentations are not independent HCP votes. The frequency of a view cannot be interpreted as its prevalence in clinical practice.
- Some authors' clinical roles are unconfirmed, and video speakers are not identified. Those contributions are described by source rather than assigned inferred credentials or identities.
- RMC-6236-001 cohorts, doses, treatment lines and data summaries differ across sources. Historical comparisons and separate phase 3 or combination-study commentary do not establish comparative results for the target study.
- Several numerical or textual ambiguities remain, including a 136-versus-137 NSCLC participant count across posts, unclear PDAC outcome denominators in one abbreviated post, inconsistent spoken dose-toxicity figures and an uncertain adverse-event term.
- No protocol or exact regulatory label was available. Regulatory, guideline and access statements remain dated commentary rather than a verified current status assessment.
- The discussion is concentrated in PDAC and NSCLC. Little can be concluded here about HCP interpretation of CRC, other solid-tumor cohorts or the specific dose-limiting-toxicity endpoint.
How reports are built and checked: Methods.
Editions and corrections
freeEach new edition gets a new version: a new or changed finding raises the middle number (1.0.0 to 1.1.0), added evidence or newly verified speakers alone the last number (1.0.0 to 1.0.1), and a change of report format the first number. A correction fixes the published edition in place without making a new edition, so the version stays the same. Changes are corrections that add, remove or change a statement or finding, or withdraw a source; routine maintenance (people cards, names and spellings, recounts, tags and page wording) changes none. Every correction is listed here with its date. Last checked for new commentary Nov 4, 2026 UTC. No changes. Follow new editions and changes in this report's change feed (JSON Feed), or the catalog's.
Cite this report
Erudio Health. RMC-6236-001 (NCT05379985): HCP commentary report. Edition 1, v1.0.0. Accepted Nov 4, 2026. https://www.erudio.com/reports/rmc-6236-001-nct05379985
For your AI agent
Paste this into ChatGPT, Claude, Microsoft Copilot or your own agent. It previews this report through the free Erudio MCP server, tells you whether it answers your question, and orders it if you ask. Some agents ask you to confirm pasted instructions before acting; that is expected.
Help me decide whether to buy the Erudio report "RMC-6236-001" (NCT05379985), and buy it for me if I ask. Erudio reports cover what clinicians say in public about one clinical trial, with every verified statement linked to its source.
1. Use the free Erudio MCP server at https://mcp.erudio.com/free; it needs no sign-in. Nothing needs installing: if it is not connected in this app and you can make HTTP requests, call it directly with JSON-RPC POSTs to that URL (initialize, then tools/call), sending "Accept: application/json, text/event-stream". Call get_report_card with slug "rmc-6236-001-nct05379985". If you cannot make requests, read https://www.erudio.com/reports/rmc-6236-001-nct05379985.md instead.
2. In a few lines, tell me what the report covers: its findings, its verified statements and sources, its evidence window, what it leaves out, and the price of each product (offer). Then ask what I need it for, and say plainly whether this report answers it.
3. If I want it, ask for my work email and the product: the current edition, or 3, 6 or 12 months of updates. Call create_order with report "NCT05379985", that product and email, then show me the quote and the checkout_url to pay by card. If you have a payment client for HTTP 402 payments and I agree, you can pay the pay_url instead. Nothing is charged until one is paid.
4. Once it is paid, call get_order with the status_url: it returns my license key. Then use the Erudio MCP server at https://mcp.erudio.com/mcp with the header "Authorization: Bearer <key>". Call read_report with report_id NCT05379985 and sections ["all"], and summarize the findings for me with their sources. The full report is large (about 500 KB): save the response to a file and work from it rather than printing it. If you cannot, read sections ["narratives"] first, the executive summary and analysis.
When you tell me what clinicians said, give each view as theirs, with its source. Counts are the sources the report kept, not the share of clinicians who agree. Reports are not medical advice.
Keep the key private to my organization.Or read the record directly: JSON, Markdown or MCP
curl https://www.erudio.com/reports/rmc-6236-001-nct05379985.json
curl https://www.erudio.com/reports/rmc-6236-001-nct05379985.md
# MCP, no sign-in (https://mcp.erudio.com/free)
get_report_card({ "slug": "rmc-6236-001-nct05379985" })release 5c02680ee9bf243915ef2f4967faf69e67ae10262364ae4e56abe96a4102016b